<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "https://jats.nlm.nih.gov/publishing/1.3/JATS-journalpublishing1-3.dtd"><article xml:lang="en" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.3" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2615-790X</journal-id><journal-title-group><journal-title>Tropical Animal Science Journal</journal-title><abbrev-journal-title>Trop. Anim. Sci. J.</abbrev-journal-title></journal-title-group><issn pub-type="epub">2615-790X</issn><issn pub-type="ppub">2615-787X</issn><publisher><publisher-name>Faculty of Animal Science, IPB University</publisher-name><publisher-loc>Indonesia</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.5398/tasj.2026.49.4.333</article-id><title-group><article-title>Non-genetic Effects and Genetic Parameters Estimation on Growth Traits of Indonesian Etawah Grade Goats</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Nugroho</surname><given-names>A. R.</given-names></name><address><country>Indonesia</country></address><xref ref-type="aff" rid="AFF-1"></xref><xref ref-type="aff" rid="AFF-3"></xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5729-1254</contrib-id><name><surname>Sumantri</surname><given-names>C.</given-names></name><address><country>Indonesia</country></address><xref ref-type="aff" rid="AFF-2"></xref></contrib><contrib contrib-type="author"><name><surname>Sutanto</surname><given-names>A.</given-names></name><address><country>Indonesia</country></address><xref ref-type="aff" rid="AFF-3"></xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2092-9645</contrib-id><name><surname>Ulum</surname><given-names>M. F.</given-names></name><address><country>Indonesia</country></address><xref ref-type="aff" rid="AFF-4"></xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0468-2443</contrib-id><name><surname>Gunawan</surname><given-names>A.</given-names></name><address><country>Indonesia</country><email>agunawan@apps.ipb.ac.id</email></address><xref rid="AFF-2" ref-type="aff"></xref><xref ref-type="corresp" rid="cor-4"></xref></contrib></contrib-group><contrib-group><contrib contrib-type="editor"><name><surname>Wiryawan</surname><given-names>Prof. Dr. Komang G</given-names></name><address><country>Indonesia</country></address><xref rid="EDITOR-AFF-1" ref-type="aff"></xref></contrib></contrib-group><aff id="AFF-1"><institution content-type="dept">Graduate School of Animal Production and Technology, Faculty of Animal Science</institution><institution-wrap><institution>IPB University</institution><institution-id institution-id-type="ror">https://ror.org/05smgpd89</institution-id></institution-wrap><country country="ID">Indonesia</country></aff><aff id="AFF-2"><institution content-type="dept">Department of Animal Production and Technology, Faculty of Animal Science</institution><institution-wrap><institution>IPB University</institution><institution-id institution-id-type="ror">https://ror.org/05smgpd89</institution-id></institution-wrap><country country="ID">Indonesia</country></aff><aff id="AFF-3"><institution content-type="dept">National Breeding Station of Pelaihari</institution><institution-wrap><institution>Ministry of Agriculture</institution><institution-id institution-id-type="ror">https://ror.org/01vfw8847</institution-id></institution-wrap><addr-line>South Borneo</addr-line><country country="LV">Indonesia</country></aff><aff id="AFF-4"><institution content-type="dept">Division of Reproduction and Obstetrics, School of Veterinary Medicine and Biomedical Sciences</institution><institution-wrap><institution>IPB University</institution><institution-id institution-id-type="ror">https://ror.org/05smgpd89</institution-id></institution-wrap><country country="ID">Indonesia</country></aff><aff id="EDITOR-AFF-1">Tropical Animal Science Journal</aff><author-notes><fn fn-type="coi-statement"><label>CONFLICT OF INTEREST</label><p>C. Sumantri and A. Gunawan serve as editors of the Tropical Animal Science Journal but have no role in the decision to publish this article. The authors state they have no competing interests.</p></fn><corresp id="cor-4">Corresponding author: A. Gunawan, Department of Animal Production and Technology, Faculty of Animal Science, IPB University, Indonesia.  Email: <email>agunawan@apps.ipb.ac.id</email></corresp></author-notes><pub-date date-type="pub" iso-8601-date="2026-6-3" publication-format="electronic"><day>3</day><month>6</month><year>2026</year></pub-date><pub-date date-type="collection" iso-8601-date="2026-6-3" publication-format="electronic"><day>3</day><month>6</month><year>2026</year></pub-date><volume>49</volume><issue>4</issue><issue-title>Tropical Animal Science Journal</issue-title><fpage>333</fpage><lpage>343</lpage><history><date iso-8601-date="2026-2-6" date-type="received"><day>6</day><month>2</month><year>2026</year></date><date date-type="rev-recd" iso-8601-date="2026-4-21"><day>21</day><month>4</month><year>2026</year></date><date date-type="accepted" iso-8601-date="2026-4-23"><day>23</day><month>4</month><year>2026</year></date></history><permissions><copyright-statement>Copyright (c) 2026 Tropical Animal Science Journal</copyright-statement><copyright-year>2026</copyright-year><copyright-holder>Tropical Animal Science Journal</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-sa/4.0/"><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">http://creativecommons.org/licenses/by-sa/4.0/</ali:license_ref><license-p>This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.Authors submitting manuscripts should understand and agree that copyright of manuscripts of the article shall be assigned/transferred to Tropical Animal Science Journal. The statement to release the copyright to Tropical Animal Science Journal is stated in Form A. This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License (CC BY-SA) where Authors and Readers can copy and redistribute the material in any medium or format, as well as remix, transform, and build upon the material for any purpose, but they must give appropriate credit (cite to the article or content), provide a link to the license, and indicate if changes were made. If you remix, transform, or build upon the material, you must distribute your contributions under the same license as the original.</license-p></license></permissions><self-uri xlink:href="https://journal.ipb.ac.id/tasj/article/view/71513" xlink:title="Non-genetic Effects and Genetic Parameters Estimation on Growth Traits of Indonesian Etawah Grade Goats">Non-genetic Effects and Genetic Parameters Estimation on Growth Traits of Indonesian Etawah Grade Goats</self-uri><abstract><p>Growth traits are important determinants of the efficiency and productivity of goat production systems. The Etawah Grade (EG) goat is a local Indonesian breed that is used for both milk and meat production. This study aimed to analyze the influence of non-genetic factors, estimate genetic parameters, and assess long-term genetic progress in growth traits of the EG goat at different ages. A total of 17,783 body weight records from 523 sires and 4342 dams were used to analyze non-genetic effects and estimate genetic parameters for growth traits in EG goats. The effect of non-genetic factors (sex, parity, season, year, and type of birth) on growth traits (body weight and average daily gain) was analyzed using a general linear model (GLM). Heritability and genetic trend were estimated using restricted maximum likelihood (REML) in the BreedR package from the R program. The results of this study showed that sex, parity, season, year, and type of birth had significant effects (p&lt;0.01) on almost all growth traits. The heritability of growth traits was classified as low to moderate heritability (0.085-0.352). The genetic correlation in this study between all traits ranged from weakly positive to strongly positive (0.10-0.88). The estimated genetic trend in this study, based on estimated breeding values (EBV), was increased for all growth traits except 8MW and ADG8. These findings could provide a comprehensive longitudinal evaluation of growth performance and genetic progress in EG goats, offering practical insights to optimize selection strategies and improve breeding program effectiveness.</p></abstract><kwd-group><kwd>body weight</kwd><kwd>etawah grade goat</kwd><kwd>genetic parameters</kwd><kwd>non-genetic factor</kwd><kwd>selection</kwd></kwd-group><custom-meta-group><custom-meta><meta-name>File created by JATS Editor</meta-name><meta-value><ext-link ext-link-type="uri" xlink:href="https://jatseditor.com" xlink:title="JATS Editor">JATS Editor</ext-link></meta-value></custom-meta><custom-meta><meta-name>issue-created-year</meta-name><meta-value>2026</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec><title>INTRODUCTION</title><p>Goats represent a strategic commodity within Indonesia’s agribusiness sector, driven by the country’s rapidly growing population. According to the Directorate General of Livestock and Animal Health Services (2024)<xref ref-type="bibr" rid="BIBR-10">(Directorate General of Livestock and Animal Health Services, 2024)</xref>, the goat population in Indonesia increased from 14,374,014 in 2023 to 15,710,055 in 2024. Goats play a significant role in fulfilling the nutritional needs of humans, particularly in rural areas<xref ref-type="bibr" rid="BIBR-21">(Gunawan et al., 2018)</xref>. Goats are widely distributed across the country, with almost 99% of goats farmed by smallholders in small-scale production, typically with 2 to 8 animals per farm<xref rid="BIBR-47" ref-type="bibr">(Sujarwanta et al., 2024)</xref>. Smallholders favor goats due to their ease of management, consistent market demand, function as a financial reserve, and frequent use in religious or cultural ceremonies. Most farmers prefer to raise local breeds, as these animals are well-adapted to Indonesia’s climate and environmental conditions<xref ref-type="bibr" rid="BIBR-41">(Rusdin et al., 2020)</xref>;<xref rid="BIBR-28" ref-type="bibr">(Khasanah et al., 2016)</xref>.</p><p>The Etawah Grade (EG) goat is an indigenous Indonesian breed, classified as a dual-purpose breed that is used for both milk and meat production (<xref ref-type="fig" rid="figure-1">Figure 1</xref>). The EG goat is originated from crossbreeding between the Jamunapari goat from India with local Indonesian goats, developed over a long period, since the Dutch colonial era. The Indonesian government has officially recognized the EG goat as a local goat breed through Ministerial Decree of Agriculture No. 695/Kpts/PD.410/2/2013. Despite this recognition, the potential of the EG goats has not been fully realized, resulting in lower production performance compared to introduced goat breeds. The development of EG goats can be achieved through breeding programs that improve their productivity, genetic quality, and economic value. Effective implementation of breeding programs requires comprehensive recording systems and complete information on various factors influencing production traits<xref ref-type="bibr" rid="BIBR-39">(Resti et al., 2024)</xref>. Estimating genetic parameters, including heritability, genetic correlation, and Estimated Breeding Value (EBV), is an essential step in selecting superior breeding stock for traits with high economic value.</p><fig id="figure-1" ignoredToc=""><label>Figure 1</label><caption><p>Etawah Grade (EG) goat</p></caption><graphic mime-subtype="jpeg" mimetype="image" xlink:href="https://journal.ipb.ac.id/tasj/article/download/71513/version/51978/33951/414682"><alt-text>Image</alt-text></graphic></fig><p>Growth traits are important production traits in goats, significantly influencing both survival and economic value. These traits are essential for assessing the potential for meat production and reproductive performance. Growth traits are determined by both genetic and non-genetic factors, including birth year, climate, birth type, sex, and parity<xref rid="BIBR-37" ref-type="bibr">(Ofori &amp; Hagan, 2020)</xref>. Non-genetic factors may mask an individual’s true genetic potential, as animal performance results from the interaction between genetic and environmental influences <xref ref-type="bibr" rid="BIBR-32">(Mamutse et al., 2023)</xref>. A better understanding of non-genetic effects on body weight traits is necessary to optimize management and improve the accuracy of estimating genetic parameters in EG goats.</p><p>Previous studies on non-genetic effects and genetic parameters have focused on several goat breeds, including Jamunapari goat<xref ref-type="bibr" rid="BIBR-9">(Dige et al., 2022)</xref>, Assam Hill goat<xref rid="BIBR-43" ref-type="bibr">(Sarma et al., 2019)</xref>, and Sirohi goat<xref ref-type="bibr" rid="BIBR-11">(Dudhe et al., 2015)</xref>. For Indonesian local goats, genetic parameter estimation has been reported for the Sapera goat<xref ref-type="bibr" rid="BIBR-4">(Anggraeni et al., 2020)</xref> and the EG goat<xref ref-type="bibr" rid="BIBR-23">(Hasan et al., 2014)</xref>. However, there is limited information regarding non-genetic effects and on genetic parameters estimation for growth traits in the Indonesian local goat, particularly the EG goat. Incorporating non-genetic factors as fixed effects in the model and using a large sample size are essential for improving the accuracy of genetic parameter estimation<xref ref-type="bibr" rid="BIBR-5">(Atoui et al., 2017)</xref>. The present study aims to analyze the influence of non-genetic factors, estimate genetic parameters, and assess long-term genetic progress for growth traits of the EG goat at different ages.</p></sec><sec><title>MATERIALS AND METHODS</title><sec><title>Data Collection and Definition of Factors</title><p>All procedures in this study were approved by the Animal Ethics Commission of IPB University (Approval No. 349–2025 IPB). The dataset comprised 17,783 body weight records, including birth weight (BW), weaning weight (WW), 6-months Weight (6MW), 8-months Weight (8MW), and 12-months Weight (12MW) (<xref rid="table-1" ref-type="table">Table 1</xref>). Data were obtained from the production records of EG goats at the National Breeding Station of Pelaihari from 2015 to 2024. The average daily gain (ADG) was calculated using the following equation:</p><p>ADG3 = (WW – BW) / D </p><p>ADG6 = (6MW – WW) / D </p><p>ADG8 = (8MW – 6WW) / D </p><p>ADG12= (12MW – 8WW) / D</p><p>ADG3 is the value of average daily gain from 0 to 3 months of age, ADG6 denotes the average daily gain from 3 to 6 months, ADG8 refers to average daily gain from 6 to 8 months, ADG12 denotes the average daily gain from 8 to 12 months, and D refers to the number of days between the second and first weighing.</p><p>The body weight and average daily gain at specific ages were analyzed to evaluate the effects of various non-genetic factors, which were categorized into levels as follows:</p><list list-type="order"><list-item><p>The season of production was classified into two categories: dry season (April-September) and rainy season (October-March).</p></list-item><list-item><p>Sex was classified into two categories: male and female.</p></list-item><list-item><p>Parity was defined as the kidding frequency of each doe, which was classified into five levels from 1 to ≥5.</p></list-item><list-item><p>The type of birth was defined as the number of kids born, which was classified into four categories: single, twin, triplet, and quadruplet.</p></list-item><list-item><p>Year of birth was classified into ten categories: from 2015 to 2024.</p></list-item></list><table-wrap id="table-1" ignoredToc=""><label>Table 1</label><caption><p>Data structure and descriptive statistics of Etawah Grade goat body weight</p></caption><table frame="box" rules="all"><thead><tr><th align="left" colspan="1" valign="middle">Category</th><th align="center" colspan="1" valign="middle">BW (kg)</th><th valign="middle" align="center" colspan="1">WW (kg)</th><th align="center" colspan="1" valign="middle">6MW (kg)</th><th colspan="1" valign="middle" align="center">8MW (kg)</th><th valign="middle" align="center" colspan="1">12MW (kg)</th><th align="center" colspan="1" valign="middle">ADG3 (kg day<sup>-1</sup>)</th><th align="center" colspan="1" valign="middle">ADG6 (kg day<sup>-1</sup>)</th><th align="center" colspan="1" valign="middle">ADG8 (kg day<sup>-1</sup>)</th><th align="center" colspan="1" valign="middle">AD12 (kg day<sup>-1</sup>)</th></tr></thead><tbody><tr><td align="left" colspan="1" valign="top">No. of animals</td><td align="center" colspan="1" valign="top">6843</td><td align="center" colspan="1" valign="top">4014</td><td align="center" colspan="1" valign="top">3669</td><td align="center" colspan="1" valign="top">1550</td><td valign="top" align="center" colspan="1">1707</td><td valign="top" align="center" colspan="1">4014</td><td valign="top" align="center" colspan="1">3626</td><td align="center" colspan="1" valign="top">1194</td><td valign="top" align="center" colspan="1">1704</td></tr><tr><td align="left" colspan="1" valign="top">No. of animals with pedigree record</td><td colspan="1" valign="top" align="center">6843</td><td align="center" colspan="1" valign="top">4014</td><td valign="top" align="center" colspan="1">3669</td><td valign="top" align="center" colspan="1">1550</td><td align="center" colspan="1" valign="top">1707</td><td align="center" colspan="1" valign="top">4014</td><td align="center" colspan="1" valign="top">3626</td><td align="center" colspan="1" valign="top">1194</td><td valign="top" align="center" colspan="1">1704</td></tr><tr><td valign="top" align="left" colspan="1">No. of sire</td><td valign="top" align="center" colspan="1">119</td><td align="center" colspan="1" valign="top">110</td><td valign="top" align="center" colspan="1">105</td><td colspan="1" valign="top" align="center">92</td><td valign="top" align="center" colspan="1">97</td><td valign="top" align="center" colspan="1">110</td><td align="center" colspan="1" valign="top">105</td><td colspan="1" valign="top" align="center">90</td><td align="center" colspan="1" valign="top">88</td></tr><tr><td colspan="1" valign="top" align="left">No. of dam</td><td align="center" colspan="1" valign="top">1057</td><td valign="top" align="center" colspan="1">952</td><td valign="top" align="center" colspan="1">939</td><td valign="top" align="center" colspan="1">710</td><td colspan="1" valign="top" align="center">684</td><td valign="top" align="center" colspan="1">952</td><td valign="top" align="center" colspan="1">928</td><td valign="top" align="center" colspan="1">625</td><td valign="top" align="center" colspan="1">684</td></tr><tr><td align="left" colspan="1" valign="top">Average progeny of sire</td><td align="center" colspan="1" valign="top">58</td><td align="center" colspan="1" valign="top">36</td><td colspan="1" valign="top" align="center">35</td><td valign="top" align="center" colspan="1">16</td><td valign="top" align="center" colspan="1">18</td><td valign="top" align="center" colspan="1">36</td><td valign="top" align="center" colspan="1">35</td><td align="center" colspan="1" valign="top">13</td><td colspan="1" valign="top" align="center">18</td></tr><tr><td valign="top" align="left" colspan="1">Average progeny of dam</td><td valign="top" align="center" colspan="1">6</td><td align="center" colspan="1" valign="top">4</td><td align="center" colspan="1" valign="top">4</td><td valign="top" align="center" colspan="1">2</td><td valign="top" align="center" colspan="1">2</td><td align="center" colspan="1" valign="top">4</td><td align="center" colspan="1" valign="top">4</td><td colspan="1" valign="top" align="center">2</td><td valign="top" align="center" colspan="1">2</td></tr><tr><td valign="top" align="left" colspan="1">Generations</td><td align="center" colspan="1" valign="top">4</td><td valign="top" align="center" colspan="1">4</td><td valign="top" align="center" colspan="1">4</td><td colspan="1" valign="top" align="center">4</td><td colspan="1" valign="top" align="center">4</td><td align="center" colspan="1" valign="top">4</td><td align="center" colspan="1" valign="top">4</td><td valign="top" align="center" colspan="1">4</td><td valign="top" align="center" colspan="1">4</td></tr><tr><td valign="top" align="left" colspan="1">Mean</td><td valign="top" align="center" colspan="1">3.491</td><td colspan="1" valign="top" align="center">14.754</td><td colspan="1" valign="top" align="center">21.223</td><td align="center" colspan="1" valign="top">26.062</td><td valign="top" align="center" colspan="1">31.062</td><td valign="top" align="center" colspan="1">0.124</td><td valign="top" align="center" colspan="1">0.090</td><td align="center" colspan="1" valign="top">0.091</td><td align="center" colspan="1" valign="top">0.068</td></tr><tr><td align="left" colspan="1" valign="top">SE</td><td align="center" colspan="1" valign="top">0.008</td><td valign="top" align="center" colspan="1">0.060</td><td valign="top" align="center" colspan="1">0.085</td><td align="center" colspan="1" valign="top">0.151</td><td valign="top" align="center" colspan="1">0.167</td><td valign="top" align="center" colspan="1">0.001</td><td align="center" colspan="1" valign="top">0.001</td><td valign="top" align="center" colspan="1">0.002</td><td valign="top" align="center" colspan="1">0.001</td></tr><tr><td valign="top" align="left" colspan="1">CV (%)</td><td align="center" colspan="1" valign="top">18.476</td><td valign="top" align="center" colspan="1">25.602</td><td align="center" colspan="1" valign="top">24.138</td><td align="center" colspan="1" valign="top">22.758</td><td align="center" colspan="1" valign="top">22.120</td><td align="center" colspan="1" valign="top">32.348</td><td align="center" colspan="1" valign="top">49.560</td><td align="center" colspan="1" valign="top">60.111</td><td valign="top" align="center" colspan="1">55.691</td></tr></tbody></table><table-wrap-foot><p>Note: BW=Birth weight, WW=Weaning weight, 6MW= 6-months weight, 8MW=8-months weight, 12MW=12-months weight, ADG3=Average daily gain from 0 to 3-months old, ADG6=Average daily gain from 3 to 6-months old, ADG8=Average daily gain from 6 to 8-months old, ADG12=Average daily gain from 8 to 12-months old SE= Standard error of mean, and CV= coefficient of variance.</p></table-wrap-foot></table-wrap></sec><sec><title>Statistical Model</title><p>Descriptive statistics, including mean, standard deviation, and standard error of mean, were calculated for all traits in the dataset. The effects of non-genetic factors (sex, parity, season, year, and type of birth) on growth traits at different ages were analyzed using a General Linear Model (GLM). Statistical analysis was conducted using the R program (version 4.5.1). Significant differences (p&lt;0.05) among the results were further analyzed using Duncan’s Multiple Range Test (DMRT). A statistical model of the GLM for the trait is described below:</p><p>Y<sub>ijklm</sub> = μ + S<sub>i</sub> + P<sub>j</sub> + SoB<sub>k</sub> + YoB<sub>1</sub> + ToB<sub>m </sub>+ <bold>ε</bold><sub>ijklm</sub></p><p>Where Y<sub>ijklm</sub> is the value of the body weight in the different ages (BW, WW, 6MW, 8MW, 12MW, ADG3, ADG6, ADG8, or ADG12), μ refers to the overall mean, S<sub>i</sub> refers to the fixed effect of sex, P<sub>j</sub> is the fixed effect of parity, SoB<sub>k</sub> represent fixed the effect of season of birth, YoB<sub>l</sub> is the fixed effect of year of birth, ToBm refers to the fixed effect of type of birth, and <bold>ε</bold><sub>ijklm</sub> is the random residual effect.</p></sec><sec><title>Estimating Genetic Parameters</title><p>Genetic parameters estimation was conducted by evaluating heritability, phenotypic correlations, and genetic correlations. Heritability is a measure of the degree to which offspring resemble their parents in performance for a trait. Phenotypic correlation measures the strength of the relationship between performance (phenotypic value) in one trait and performance in another trait. Genetic correlation measures the strength of the relationship between breeding values for one trait and breeding values for another trait. The characteristics of the pedigree and data structure for all growth traits are listed in <xref ref-type="table" rid="table-1">Table 1</xref>. All animals included in the analysis had complete pedigree records, reflecting a high level of pedigree completeness. The dataset included a substantial number of records per trait, and the average number of progenies per sire or dam was sufficient to estimate genetic parameters. The relatively high number of progenies per sire indicates a strong contribution of sires to the population structure, which is beneficial for accurate genetic evaluation.</p><p>The estimation of (co)variance components was conducted using the model with Restricted Maximum Likelihood (REML), applying the BreedR package from the R program (version 4.5.1). The mixed-model equation for estimating genetic parameters of production traits was referred to Walsh &amp; Lynch (2018)<xref rid="BIBR-50" ref-type="bibr">(Walsh &amp; Lynch, 2018)</xref>:</p><p>Y = X<bold><italic>β</italic></bold> + <italic>Za</italic> + <italic>e</italic></p><p>Where Y is the vector of observations (BW, WW, 6MW, 8MW, 12MW, ADG3, ADG6, ADG8, or ADG12), <bold><italic>β</italic></bold> is the vector of the fixed effect (sex, parity, season, year, and type of birth), <italic>a</italic> is the vector related to random additive genetic effect of the animal, X and Z are the incidence matrices relating to observations of the factors in the model, and <italic>e</italic> is the residual effect.</p><p>The heritability for each trait was calculated based on Alam <italic>et al.</italic> (2021)<xref rid="BIBR-2" ref-type="bibr">(Alam et al., 2021)</xref>, while phenotypic and genetic correlation were calculated based on Bourdon (2014)<xref ref-type="bibr" rid="BIBR-7">(Bourdon, 2014)</xref>:</p><p>Heritability:</p><p><inline-formula><tex-math id="math-1"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle h^2=\frac{\sigma_a^2}{\sigma_p^2}\ \text{where,}\ \sigma_p^2=\sigma_a^2+\sigma_e^2 \end{document} ]]></tex-math></inline-formula></p><p>Where <inline-formula><tex-math id="math-2"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_a^2 \end{document} ]]></tex-math></inline-formula> refers to the additive genetic variance of the animal, <inline-formula><tex-math id="math-3"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_p^2 \end{document} ]]></tex-math></inline-formula> refers to the phenotypic variance, and <inline-formula><tex-math id="math-4"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_e^2 \end{document} ]]></tex-math></inline-formula> refers to residual variance.</p><p>Phenotypic correlation:</p><p><inline-formula><tex-math id="math-5"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle r_p=\frac{\mathrm{COV}_{p(XY)}}{\sigma_{px}\,\sigma_{py}} \end{document} ]]></tex-math></inline-formula></p><p>Genetic correlation:</p><p><inline-formula><tex-math id="math-6"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle r_g=\frac{\mathrm{COV}_{g(XY)}}{\sigma_{gx}\,\sigma_{gy}} \end{document} ]]></tex-math></inline-formula></p><p>COV<sub>p</sub>(XY) and COV<sub>g</sub>(XY) refer to the phenotypic and genetic covariances between the two traits. Meanwhile, σ<sub>p</sub>X and σ<sub>g</sub>X refer to the phenotypic and additive genetic standard deviations of the first trait, whereas σ<sub>p</sub>Y and σ<sub>g</sub>Y refer to the phenotypic and additive genetic standard deviations of the second trait.</p><p>The genetic trend was estimated to evaluate the genetic progress achieved during the years of observation. Genetic trend evaluation was conducted by creating a trend plot of EBV means for each trait as a function of birth year. The breeding values of individual animals were estimated using BLUP in the R program (version 4.5.1) using the BreedR package.</p></sec></sec><sec><title>RESULTS</title><sec><title>Non-Genetic Effect</title><p>The descriptive statistic showed the value of mean and standard error of BW, WW, 6MW, 8MW, and 12MW of Etawah Grade goat were 3.491±0.008 kg (CV=18.476%); 14.754±0.060 kg (CV=25.602%); 21.223±0.085 kg (CV=24.138%); 26.062±0.151 kg (CV=22.758%); and 31.062±0.167 kg (CV=22.120%), respectively (<xref ref-type="table" rid="table-1">Table 1</xref>). The overall value of mean and standard error of ADG3, ADG6, ADG8, and ADG12 of EG goat were 0.124±0.001 kg day<sup>-1</sup> (CV=32.348%); 0.090±0.001 kg day<sup>-1</sup> (CV=49.560%); 0.091±0.002 kg day<sup>-1</sup> (CV=60.111%); and 0.068±0.001 kg day<sup>-1</sup> (CV=55.691%), respectively (<xref ref-type="table" rid="table-1">Table 1</xref>). The result of this study showed that sex, parity, season, year, and type of birth had a highly significant effect (p&lt;0.01) on all body weight traits in this study, except for season of birth, which was not significant (p&gt;0.05) for 8MW (<xref ref-type="table" rid="table-2">Table 2</xref>). For ADG traits, sex, parity, season, year, and type of birth had a significant effect (p&lt;0.05) on ADG3 and ADG6 (<xref ref-type="table" rid="table-3">Table 3</xref>). ADG8 was only affected (p&gt;0.05) by sex, year, and type of birth. ADG12 in this study was affected (p&gt;0.05) by sex, season, and year of birth.</p><table-wrap id="table-2" ignoredToc=""><label>Table 2</label><caption><p>Body weight (kg) of Etawah Grade (EG) goat at a specific age (Mean ± SE)</p></caption><table frame="box" rules="all"><thead><tr><th align="left" colspan="2" rowspan="2" valign="middle">Factor</th><th align="center" colspan="10" valign="top">Body weight at a specific age</th></tr><tr><th align="center" colspan="1" valign="top">n</th><th align="center" colspan="1" valign="top">BW</th><th valign="top" align="center" colspan="1">n</th><th colspan="1" valign="top" align="center">WW</th><th align="center" colspan="1" valign="top">n</th><th align="center" colspan="1" valign="top">6MW</th><th align="center" colspan="1" valign="top">n</th><th valign="top" align="center" colspan="1">8MW</th><th align="center" colspan="1" valign="top">n</th><th valign="top" align="center" colspan="1">12MW</th></tr></thead><tbody><tr><td align="left" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1"></td><td colspan="1" valign="top" align="center">**</td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td colspan="1" valign="top" align="center">**</td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1">**</td></tr><tr><td colspan="1" rowspan="2" valign="top" align="left">Season</td><td align="center" colspan="1" valign="top">Rainy</td><td valign="top" align="center" colspan="1">3395</td><td valign="top" align="center" colspan="1">3.51±0.011ᵃ</td><td align="center" colspan="1" valign="top">2004</td><td colspan="1" valign="top" align="center">15.09±0.069ᵃ</td><td valign="top" align="center" colspan="1">1808</td><td valign="top" align="center" colspan="1">21.78±0.095ᵃ</td><td align="center" colspan="1" valign="top">680</td><td align="center" colspan="1" valign="top">25.77±0.160ᵇ</td><td valign="top" align="center" colspan="1">884</td><td valign="top" align="center" colspan="1">30.54±0.179ᵇ</td></tr><tr><td valign="top" align="center" colspan="1">Dry</td><td align="center" colspan="1" valign="top">3448</td><td valign="top" align="center" colspan="1">3.47±0.011ᵇ</td><td colspan="1" valign="top" align="center">2010</td><td align="center" colspan="1" valign="top">14.41±0.069ᵇ</td><td valign="top" align="center" colspan="1">1861</td><td valign="top" align="center" colspan="1">20.99±0.093ᵇ</td><td valign="top" align="center" colspan="1">835</td><td align="center" colspan="1" valign="top">26.36±0.178ᵃ</td><td valign="top" align="center" colspan="1">732</td><td valign="top" align="center" colspan="1">31.47±0.163ᵃ</td></tr><tr><td valign="top" align="left" colspan="1"></td><td colspan="1" valign="top" align="center"></td><td colspan="1" valign="top" align="center"></td><td align="center" colspan="1" valign="top">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td colspan="1" valign="top" align="center"></td><td colspan="1" valign="top" align="center">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td valign="top" align="center" colspan="1"></td><td colspan="1" valign="top" align="center">**</td></tr><tr><td rowspan="2" valign="top" align="left" colspan="1">Sex</td><td valign="top" align="center" colspan="1">Male</td><td valign="top" align="center" colspan="1">3342</td><td align="center" colspan="1" valign="top">3.63±0.009ᵃ</td><td valign="top" align="center" colspan="1">2044</td><td align="center" colspan="1" valign="top">15.46±0.070ᵃ</td><td align="center" colspan="1" valign="top">1867</td><td valign="top" align="center" colspan="1">22.55±0.095ᵃ</td><td valign="top" align="center" colspan="1">855</td><td align="center" colspan="1" valign="top">27.66±0.180ᵃ</td><td valign="top" align="center" colspan="1">481</td><td align="center" colspan="1" valign="top">32.72±0.220ᵃ</td></tr><tr><td valign="top" align="center" colspan="1">Female</td><td valign="top" align="center" colspan="1">3501</td><td colspan="1" valign="top" align="center">3.35±0.009ᵇ</td><td valign="top" align="center" colspan="1">2078</td><td align="center" colspan="1" valign="top">14.06±0.069ᵇ</td><td align="center" colspan="1" valign="top">1927</td><td align="center" colspan="1" valign="top">19.96±0.093ᵇ</td><td valign="top" align="center" colspan="1">660</td><td align="center" colspan="1" valign="top">24.78±0.159ᵇ</td><td valign="top" align="center" colspan="1">1135</td><td valign="top" align="center" colspan="1">30.35±0.143ᵇ</td></tr><tr><td align="left" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1">**</td><td align="center" colspan="1" valign="top"></td><td align="center" colspan="1" valign="top">**</td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td valign="top" align="center" colspan="1"></td><td colspan="1" valign="top" align="center">**</td></tr><tr><td valign="top" align="left" colspan="1" rowspan="4">Birth type</td><td valign="top" align="center" colspan="1">Single</td><td valign="top" align="center" colspan="1">1176</td><td valign="top" align="center" colspan="1">3.89±0.019ᵃ</td><td valign="top" align="center" colspan="1">756</td><td valign="top" align="center" colspan="1">16.19±0.112ᵃ</td><td valign="top" align="center" colspan="1">672</td><td valign="top" align="center" colspan="1">22.31±0.156ᵃ</td><td align="center" colspan="1" valign="top">313</td><td align="center" colspan="1" valign="top">26.92±0.262ᵃ</td><td align="center" colspan="1" valign="top">385</td><td valign="top" align="center" colspan="1">31.16±0.246ᵃ</td></tr><tr><td valign="top" align="center" colspan="1">Twin</td><td align="center" colspan="1" valign="top">4174</td><td align="center" colspan="1" valign="top">3.55±0.009ᵇ</td><td valign="top" align="center" colspan="1">2473</td><td valign="top" align="center" colspan="1">14.50±0.062ᵇ</td><td align="center" colspan="1" valign="top">2239</td><td valign="top" align="center" colspan="1">20.95±0.086ᵇ</td><td align="center" colspan="1" valign="top">911</td><td align="center" colspan="1" valign="top">25.74±0.153ᵃ</td><td align="center" colspan="1" valign="top">1001</td><td align="center" colspan="1" valign="top">31.87±0.152ᵃ</td></tr><tr><td colspan="1" valign="top" align="center">Triplet</td><td colspan="1" valign="top" align="center">1393</td><td valign="top" align="center" colspan="1">3.02±0.013<sup>c</sup></td><td align="center" colspan="1" valign="top">749</td><td valign="top" align="center" colspan="1">14.21±0.113ᵇ</td><td valign="top" align="center" colspan="1">726</td><td align="center" colspan="1" valign="top">21.16±0.150ᵇ</td><td valign="top" align="center" colspan="1">278</td><td align="center" colspan="1" valign="top">26.10±0.278ᵃ</td><td colspan="1" valign="top" align="center">212</td><td valign="top" align="center" colspan="1">31.99±0.332ᵃ</td></tr><tr><td colspan="1" valign="top" align="center">Quadruplet</td><td valign="top" align="center" colspan="1">100</td><td valign="top" align="center" colspan="1">2.60±0.042ᵈ</td><td colspan="1" valign="top" align="center">36</td><td align="center" colspan="1" valign="top">13.05±0.517<sup>c</sup></td><td align="center" colspan="1" valign="top">32</td><td colspan="1" valign="top" align="center">18.74±0.713<sup>c</sup></td><td valign="top" align="center" colspan="1">13</td><td align="center" colspan="1" valign="top">23.14±1.2857ᵇ</td><td align="center" colspan="1" valign="top">18</td><td valign="top" align="center" colspan="1">27.86±1.139ᵇ</td></tr><tr><td valign="top" align="left" colspan="1"></td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td colspan="1" valign="top" align="center"></td><td colspan="1" valign="top" align="center">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td align="center" colspan="1" valign="top"></td><td align="center" colspan="1" valign="top">**</td></tr><tr><td align="left" colspan="1" rowspan="5" valign="top">Parity</td><td valign="top" align="center" colspan="1">1</td><td valign="top" align="center" colspan="1">1162</td><td valign="top" align="center" colspan="1">3.46±0.016ᵇ</td><td valign="top" align="center" colspan="1">655</td><td valign="top" align="center" colspan="1">15.35±0.121ᵃ</td><td valign="top" align="center" colspan="1">660</td><td valign="top" align="center" colspan="1">21.70±0.157ᵃ</td><td align="center" colspan="1" valign="top">323</td><td valign="top" align="center" colspan="1">26.59±0.265ᵃ</td><td align="center" colspan="1" valign="top">293</td><td valign="top" align="center" colspan="1">31.88±0.281ᵃ</td></tr><tr><td valign="top" align="center" colspan="1">2</td><td valign="top" align="center" colspan="1">1466</td><td colspan="1" valign="top" align="center">3.52±0.014ᵃ</td><td colspan="1" valign="top" align="center">893</td><td valign="top" align="center" colspan="1">15.09±0.104<sup>ab</sup></td><td align="center" colspan="1" valign="top">802</td><td valign="top" align="center" colspan="1">21.31±0.142ᵃᵇ</td><td valign="top" align="center" colspan="1">339</td><td valign="top" align="center" colspan="1">26.21±0.255ᵃ</td><td align="center" colspan="1" valign="top">365</td><td align="center" colspan="1" valign="top">30.93±0.251<sup>bc</sup></td></tr><tr><td valign="top" align="center" colspan="1">3</td><td align="center" colspan="1" valign="top">1382</td><td valign="top" align="center" colspan="1">3.53±0.014ᵃ</td><td align="center" colspan="1" valign="top">804</td><td align="center" colspan="1" valign="top">14.82±0.109ᵇ</td><td align="center" colspan="1" valign="top">723</td><td align="center" colspan="1" valign="top">21.46±0.150ᵃ</td><td valign="top" align="center" colspan="1">272</td><td align="center" colspan="1" valign="top">26.31±0.282ᵃ</td><td valign="top" align="center" colspan="1">379</td><td align="center" colspan="1" valign="top">30.92±0.247<sup>bc</sup></td></tr><tr><td valign="top" align="center" colspan="1">4</td><td colspan="1" valign="top" align="center">1174</td><td align="center" colspan="1" valign="top">3.45±0.016ᵇ</td><td colspan="1" valign="top" align="center">687</td><td valign="top" align="center" colspan="1">14.42±0.118<sup>c</sup></td><td valign="top" align="center" colspan="1">652</td><td align="center" colspan="1" valign="top">20.74±0.158<sup>c</sup></td><td align="center" colspan="1" valign="top">241</td><td valign="top" align="center" colspan="1">25.00±0.300ᵇ</td><td valign="top" align="center" colspan="1">312</td><td align="center" colspan="1" valign="top">31.29±0.272<sup>ab</sup></td></tr><tr><td colspan="1" valign="top" align="center">≥5</td><td valign="top" align="center" colspan="1">1659</td><td valign="top" align="center" colspan="1">3.48±0.013ᵇ</td><td valign="top" align="center" colspan="1">975</td><td align="center" colspan="1" valign="top">14.22±0.100<sup>c</sup></td><td valign="top" align="center" colspan="1">832</td><td align="center" colspan="1" valign="top">20.95±0.140bc</td><td colspan="1" valign="top" align="center">375</td><td valign="top" align="center" colspan="1">25.85±0.240ᵃ</td><td align="center" colspan="1" valign="top">358</td><td valign="top" align="center" colspan="1">30.49±0.253<sup>c</sup></td></tr><tr><td align="left" colspan="1" valign="top"></td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1">**</td><td colspan="1" valign="top" align="center"></td><td valign="top" align="center" colspan="1">**</td><td colspan="1" valign="top" align="center"></td><td valign="top" align="center" colspan="1">**</td></tr><tr><td colspan="1" rowspan="10" valign="top" align="left">Year</td><td colspan="1" valign="top" align="center">2015</td><td align="center" colspan="1" valign="top">262</td><td colspan="1" valign="top" align="center">3.56±0.033ᵃ</td><td colspan="1" valign="top" align="center">141</td><td colspan="1" valign="top" align="center">13.14±0.261ᵉ</td><td align="center" colspan="1" valign="top">131</td><td colspan="1" valign="top" align="center">16.86±0.352ᵉ</td><td align="center" colspan="1" valign="top">27</td><td valign="top" align="center" colspan="1">19.87±0.892<sup>ef</sup></td><td align="center" colspan="1" valign="top">119</td><td valign="top" align="center" colspan="1">27.00±0.443ᵈ</td></tr><tr><td valign="top" align="center" colspan="1">2016</td><td valign="top" align="center" colspan="1">325</td><td align="center" colspan="1" valign="top">3.48±0.030<sup>bc</sup></td><td valign="top" align="center" colspan="1">187</td><td valign="top" align="center" colspan="1">13.26±0.227ᵉ</td><td align="center" colspan="1" valign="top">221</td><td valign="top" align="center" colspan="1">19.42±0.271ᵈ</td><td align="center" colspan="1" valign="top">30</td><td colspan="1" valign="top" align="center">20.62±0.846ᵉ</td><td colspan="1" valign="top" align="center">157</td><td valign="top" align="center" colspan="1">30.89±0.386<sup>c</sup></td></tr><tr><td valign="top" align="center" colspan="1">2017</td><td valign="top" align="center" colspan="1">528</td><td valign="top" align="center" colspan="1">3.43±0.023<sup>cd</sup></td><td align="center" colspan="1" valign="top">382</td><td valign="top" align="center" colspan="1">12.82±0.159ᵉ</td><td valign="top" align="center" colspan="1">202</td><td colspan="1" valign="top" align="center">16.01±0.283<sup>f</sup></td><td align="center" colspan="1" valign="top">96</td><td align="center" colspan="1" valign="top">18.85±0.473<sup>fg</sup></td><td valign="top" align="center" colspan="1">243</td><td valign="top" align="center" colspan="1">25.43±0.310<sup>de</sup></td></tr><tr><td valign="top" align="center" colspan="1">2018</td><td valign="top" align="center" colspan="1">534</td><td valign="top" align="center" colspan="1">3.59±0.023ᵃ</td><td valign="top" align="center" colspan="1">356</td><td valign="top" align="center" colspan="1">11.71±0.164<sup>f</sup></td><td valign="top" align="center" colspan="1">227</td><td align="center" colspan="1" valign="top">14.93±0.268ᵍ</td><td valign="top" align="center" colspan="1">48</td><td valign="top" align="center" colspan="1">17.87±0.669ᵍ</td><td valign="top" align="center" colspan="1">162</td><td colspan="1" valign="top" align="center">24.12±0.380ᵉ</td></tr><tr><td align="center" colspan="1" valign="top">2019</td><td colspan="1" valign="top" align="center">539</td><td align="center" colspan="1" valign="top">3.37±0.023ᵈ</td><td valign="top" align="center" colspan="1">454</td><td valign="top" align="center" colspan="1">14.68±0.145<sup>c</sup></td><td valign="top" align="center" colspan="1">363</td><td valign="top" align="center" colspan="1">21.67±0.211ᵇ</td><td align="center" colspan="1" valign="top">153</td><td colspan="1" valign="top" align="center">24.22±0.375ᵈ</td><td valign="top" align="center" colspan="1">223</td><td align="center" colspan="1" valign="top">31.24±0.324<sup>c</sup></td></tr><tr><td valign="top" align="center" colspan="1">2020</td><td align="center" colspan="1" valign="top">647</td><td colspan="1" valign="top" align="center">3.59±0.021ᵃ</td><td valign="top" align="center" colspan="1">353</td><td align="center" colspan="1" valign="top">14.69±0.165<sup>c</sup></td><td valign="top" align="center" colspan="1">374</td><td valign="top" align="center" colspan="1">20.08±0.208<sup>c</sup></td><td align="center" colspan="1" valign="top">211</td><td align="center" colspan="1" valign="top">25.31±0.319<sup>cd</sup></td><td valign="top" align="center" colspan="1">99</td><td valign="top" align="center" colspan="1">32.57±0.486<sup>c</sup></td></tr><tr><td valign="top" align="center" colspan="1">2021</td><td valign="top" align="center" colspan="1">873</td><td valign="top" align="center" colspan="1">3.54±0.018<sup>ab</sup></td><td colspan="1" valign="top" align="center">348</td><td valign="top" align="center" colspan="1">17.37±0.166ᵃ</td><td align="center" colspan="1" valign="top">498</td><td valign="top" align="center" colspan="1">23.69±0.181ᵃ</td><td colspan="1" valign="top" align="center">251</td><td align="center" colspan="1" valign="top">28.51±0.292ᵃ</td><td align="center" colspan="1" valign="top">206</td><td valign="top" align="center" colspan="1">32.90±0.337<sup>c</sup></td></tr><tr><td align="center" colspan="1" valign="top">2022</td><td valign="top" align="center" colspan="1">1094</td><td valign="top" align="center" colspan="1">3.46±0.016<sup>c</sup></td><td valign="top" align="center" colspan="1">607</td><td valign="top" align="center" colspan="1">15.48±0.126ᵇ</td><td valign="top" align="center" colspan="1">642</td><td valign="top" align="center" colspan="1">22.07±0.159ᵇ</td><td align="center" colspan="1" valign="top">261</td><td align="center" colspan="1" valign="top">27.31±0.287<sup>ab</sup></td><td valign="top" align="center" colspan="1">223</td><td valign="top" align="center" colspan="1">35.55±0.323ᵇ</td></tr><tr><td align="center" colspan="1" valign="top">2023</td><td valign="top" align="center" colspan="1">978</td><td align="center" colspan="1" valign="top">3.48±0.017<sup>bc</sup></td><td colspan="1" valign="top" align="center">672</td><td align="center" colspan="1" valign="top">16.96±0.119ᵃ</td><td valign="top" align="center" colspan="1">639</td><td valign="top" align="center" colspan="1">24.34±0.160ᵃ</td><td valign="top" align="center" colspan="1">322</td><td valign="top" align="center" colspan="1">28.77±0.258ᵃ</td><td align="center" colspan="1" valign="top">177</td><td align="center" colspan="1" valign="top">39.04±0.363ᵃ</td></tr><tr><td align="center" colspan="1" valign="top">2024</td><td valign="top" align="center" colspan="1">1063</td><td valign="top" align="center" colspan="1">3.46±0.016<sup>c</sup></td><td align="center" colspan="1" valign="top">514</td><td align="center" colspan="1" valign="top">13.87±0.137ᵈ</td><td align="center" colspan="1" valign="top">372</td><td align="center" colspan="1" valign="top">21.96±0.209<sup>c</sup></td><td valign="top" align="center" colspan="1">116</td><td colspan="1" valign="top" align="center">26.04±0.430<sup>bc</sup></td><td align="center" colspan="1" valign="top">7</td><td align="center" colspan="1" valign="top">32.20±1.826<sup>c</sup></td></tr></tbody></table><table-wrap-foot><p>Note: BW=Birth weight, WW=Weaning weight, 6MW= 6-months weight, 8MW=8-months weight, 12MW=12-months weight. Means in the same column with different superscript differ significantly (* = p&lt;0.05) or (** = p&lt;0.01).</p></table-wrap-foot></table-wrap></sec><sec><title>Estimated Heritability</title><p>The variance components for all traits were estimated by assessing the effects of sex, parity, season, year, and birth type. Among all body weights, BW showed the lowest estimated additive genetic value (0.100). The estimated additive genetic variance increased with age, with values of 3.219 for WW, 7.439 for 6MW, 6.893 for 8MW, and 7.661 for 12MW. In contrast, average daily gain traits showed very low additive genetic variance, ranging from 0.0001 to 0.0004. The estimated phenotypic variance of body weight increased continuously with advancing age of the animals, showing a pattern similar to that of additive genetic variance. However, the phenotypic variance of average daily gain traits did not follow this pattern, with the highest value observed at ADG8 (0.0024) and the lowest at ADG12 (0.0011). The heritability of BW, WW, 6MW, 8MW, and 12MW were estimated to be 0.314±0.028; 0.265±0.034; 0.352±0.038; 0.273±0.054; and 0.254±0.052, respectively (<xref ref-type="table" rid="table-3">Table 3</xref>). The heritability estimates for ADG3, ADG6, ADG8, and ADG12 in this study were 0.254±0.034; 0.135±0.029; 0.161±0.053; and 0.085±0.034, respectively (<xref ref-type="table" rid="table-3">Table 3</xref>).</p><table-wrap id="table-3" ignoredToc=""><label>Table 3</label><caption><p>Average daily gain (kg day-1) of Etawah Grade (EG) goat at a specific age (Mean ± SE)</p></caption><table frame="box" rules="all"><thead><tr><th rowspan="2" valign="middle" align="left" colspan="2">Factors</th><th align="center" colspan="8" valign="top">Average daily gain at a specific age</th></tr><tr><th valign="top" align="center" colspan="1"><underline>n</underline></th><th align="center" colspan="1" valign="top">ADG3</th><th valign="top" align="center" colspan="1">n</th><th valign="top" align="center" colspan="1">ADG6</th><th align="center" colspan="1" valign="top"><underline>n</underline></th><th valign="top" align="center" colspan="1">ADG8</th><th valign="top" align="center" colspan="1"><underline>n</underline></th><th align="center" colspan="1" valign="top">ADG12</th></tr></thead><tbody><tr><td valign="top" align="left" colspan="1"></td><td valign="top" align="left" colspan="1"></td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td align="center" colspan="1" valign="top"></td><td align="center" colspan="1" valign="top">**</td><td align="center" colspan="1" valign="top"></td><td align="center" colspan="1" valign="top">**</td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1">**</td></tr><tr><td align="left" colspan="1" rowspan="2" valign="top">Season</td><td colspan="1" valign="top" align="center">Rainy</td><td align="center" colspan="1" valign="top">2004</td><td colspan="1" valign="top" align="center">0.128±0.001ᵃ</td><td colspan="1" valign="top" align="center">1787</td><td colspan="1" valign="top" align="center">0.094±0.069ᵃ</td><td valign="top" align="center" colspan="1">673</td><td valign="top" align="center" colspan="1">0.090±0.002ᵇ</td><td valign="top" align="center" colspan="1">891</td><td valign="top" align="center" colspan="1">0.64±0.001ᵃ</td></tr><tr><td valign="top" align="center" colspan="1">Dry</td><td align="center" colspan="1" valign="top">2010</td><td valign="top" align="center" colspan="1">0.120±0.001ᵇ</td><td align="center" colspan="1" valign="top">1839</td><td align="center" colspan="1" valign="top">0.087±0.069ᵇ</td><td valign="top" align="center" colspan="1">521</td><td valign="top" align="center" colspan="1">0.091±0.002ᵃ</td><td colspan="1" valign="top" align="center">505</td><td valign="top" align="center" colspan="1">0.078±0.001ᵇ</td></tr><tr><td valign="top" align="left" colspan="1"></td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td colspan="1" valign="top" align="center">**</td></tr><tr><td rowspan="2" valign="top" align="left" colspan="1">Sex</td><td valign="top" align="center" colspan="1">Male</td><td valign="top" align="center" colspan="1">1981</td><td align="center" colspan="1" valign="top">0.130±0.001ᵃ</td><td valign="top" align="center" colspan="1">1781</td><td valign="top" align="center" colspan="1">0.100±0.001ᵃ</td><td align="center" colspan="1" valign="top">518</td><td valign="top" align="center" colspan="1">0.099±0.002ᵃ</td><td align="center" colspan="1" valign="top">855</td><td colspan="1" valign="top" align="center">27.66±0.180ᵃ</td></tr><tr><td valign="top" align="center" colspan="1">Female</td><td align="center" colspan="1" valign="top">2033</td><td align="center" colspan="1" valign="top">0.118±0.001ᵇ</td><td valign="top" align="center" colspan="1">1845</td><td align="center" colspan="1" valign="top">0.081±0.001ᵇ</td><td valign="top" align="center" colspan="1">676</td><td valign="top" align="center" colspan="1">0.085±0.002ᵇ</td><td valign="top" align="center" colspan="1">660</td><td align="center" colspan="1" valign="top">24.78±0.159ᵇ</td></tr><tr><td valign="top" align="left" colspan="1"></td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1"></td></tr><tr><td valign="top" align="left" colspan="1" rowspan="4">Birth type</td><td valign="top" align="center" colspan="1">Single</td><td align="center" colspan="1" valign="top">756</td><td align="center" colspan="1" valign="top">0.135±0.001ᵃ</td><td align="center" colspan="1" valign="top">669</td><td align="center" colspan="1" valign="top">0.102±0.002ᵃ</td><td align="center" colspan="1" valign="top">248</td><td align="center" colspan="1" valign="top">0.090±0.003ᵇ</td><td valign="top" align="center" colspan="1">385</td><td colspan="1" valign="top" align="center">0.066±0.002</td></tr><tr><td valign="top" align="center" colspan="1">Twin</td><td colspan="1" valign="top" align="center">2473</td><td align="center" colspan="1" valign="top">0.121±0.001ᵇ</td><td align="center" colspan="1" valign="top">2211</td><td valign="top" align="center" colspan="1">0.088±0.008ᵇ</td><td valign="top" align="center" colspan="1">722</td><td align="center" colspan="1" valign="top">0.090±0.002ᵇ</td><td align="center" colspan="1" valign="top">1089</td><td colspan="1" valign="top" align="center">0.068±0.001</td></tr><tr><td colspan="1" valign="top" align="center">Triplet</td><td valign="top" align="center" colspan="1">749</td><td valign="top" align="center" colspan="1">0.124±0.001ᵇ</td><td colspan="1" valign="top" align="center">714</td><td valign="top" align="center" colspan="1">0.088±0.001ᵇ</td><td align="center" colspan="1" valign="top">216</td><td align="center" colspan="1" valign="top">0.090±0.003ᵇ</td><td valign="top" align="center" colspan="1">212</td><td valign="top" align="center" colspan="1">0.070±0.002</td></tr><tr><td colspan="1" valign="top" align="center">Quadruplet</td><td valign="top" align="center" colspan="1">36</td><td valign="top" align="center" colspan="1">0.115±0.006ᵇ</td><td align="center" colspan="1" valign="top">32</td><td valign="top" align="center" colspan="1">0.66±0.007<sup>c</sup></td><td colspan="1" valign="top" align="center">8</td><td valign="top" align="center" colspan="1">0.114±0.017ᵃ</td><td colspan="1" valign="top" align="center">18</td><td align="center" colspan="1" valign="top">0.068±0.008</td></tr><tr><td align="left" colspan="1" valign="top"></td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">*</td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top"></td><td colspan="1" valign="top" align="center"></td></tr><tr><td colspan="1" rowspan="5" valign="top" align="left">Parity</td><td colspan="1" valign="top" align="center">1</td><td align="center" colspan="1" valign="top">655</td><td valign="top" align="center" colspan="1">0.131±0.001ᵃ</td><td valign="top" align="center" colspan="1">656</td><td valign="top" align="center" colspan="1">0.093±0.002ᵃ</td><td align="center" colspan="1" valign="top">239</td><td valign="top" align="center" colspan="1">0.090±0.003</td><td align="center" colspan="1" valign="top">292</td><td valign="top" align="center" colspan="1">0.066±0.002</td></tr><tr><td valign="top" align="center" colspan="1">2</td><td colspan="1" valign="top" align="center">893</td><td align="center" colspan="1" valign="top">0.128±0.001ᵇ</td><td align="center" colspan="1" valign="top">789</td><td valign="top" align="center" colspan="1">0.093±0.001ᵃ</td><td align="center" colspan="1" valign="top">248</td><td align="center" colspan="1" valign="top">0.097±0.003</td><td align="center" colspan="1" valign="top">364</td><td align="center" colspan="1" valign="top">0.066±0.002</td></tr><tr><td valign="top" align="center" colspan="1">3</td><td valign="top" align="center" colspan="1">804</td><td align="center" colspan="1" valign="top">0.124±0.001<sup>c</sup></td><td align="center" colspan="1" valign="top">714</td><td valign="top" align="center" colspan="1">0.091±0.001<sup>ab</sup></td><td valign="top" align="center" colspan="1">202</td><td align="center" colspan="1" valign="top">0.089±0.003</td><td valign="top" align="center" colspan="1">378</td><td align="center" colspan="1" valign="top">0.070±0.002</td></tr><tr><td valign="top" align="center" colspan="1">4</td><td align="center" colspan="1" valign="top">687</td><td valign="top" align="center" colspan="1">0.121±0.001ᵈ</td><td valign="top" align="center" colspan="1">647</td><td valign="top" align="center" colspan="1">0.088±0.002ᵇ</td><td align="center" colspan="1" valign="top">192</td><td align="center" colspan="1" valign="top">0.084±0.004</td><td valign="top" align="center" colspan="1">312</td><td colspan="1" valign="top" align="center">0.070±0.002</td></tr><tr><td align="center" colspan="1" valign="top">≥5</td><td valign="top" align="center" colspan="1">975</td><td valign="top" align="center" colspan="1">0.119±0.001ᵈ</td><td valign="top" align="center" colspan="1">820</td><td valign="top" align="center" colspan="1">0.087±0.001ᵇ</td><td valign="top" align="center" colspan="1">313</td><td align="center" colspan="1" valign="top">0.090±0.002</td><td align="center" colspan="1" valign="top">358</td><td valign="top" align="center" colspan="1">0.067±0.002</td></tr><tr><td valign="top" align="left" colspan="1"></td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td><td align="center" colspan="1" valign="top"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td valign="top" align="center" colspan="1">**</td><td valign="top" align="center" colspan="1"></td><td align="center" colspan="1" valign="top">**</td></tr><tr><td colspan="1" rowspan="10" valign="top" align="left">Year</td><td valign="top" align="center" colspan="1">2015</td><td valign="top" align="center" colspan="1">141</td><td valign="top" align="center" colspan="1">0.105±0.003ᵉ</td><td colspan="1" valign="top" align="center">130</td><td align="center" colspan="1" valign="top">0.065±0.003ᵉ</td><td valign="top" align="center" colspan="1">25</td><td valign="top" align="center" colspan="1">0.049±0.010ᵈ</td><td valign="top" align="center" colspan="1">119</td><td valign="top" align="center" colspan="1">0.060±0.003ᵇ</td></tr><tr><td valign="top" align="center" colspan="1">2016</td><td colspan="1" valign="top" align="center">187</td><td align="center" colspan="1" valign="top">0.108±0.002ᵉ</td><td colspan="1" valign="top" align="center">221</td><td align="center" colspan="1" valign="top">0.080±0.003ᵈ</td><td valign="top" align="center" colspan="1">29</td><td valign="top" align="center" colspan="1">0.047±0.009ᵈ</td><td valign="top" align="center" colspan="1">157</td><td valign="top" align="center" colspan="1">0.072±0.003ᵇ</td></tr><tr><td valign="top" align="center" colspan="1">2017</td><td valign="top" align="center" colspan="1">382</td><td align="center" colspan="1" valign="top">0.104±0.001ᵉ</td><td align="center" colspan="1" valign="top">198</td><td valign="top" align="center" colspan="1">0.057±0.003<sup>f</sup></td><td valign="top" align="center" colspan="1">76</td><td align="center" colspan="1" valign="top">0.042±0.00ᵈ</td><td valign="top" align="center" colspan="1">243</td><td valign="top" align="center" colspan="1">0.045±0.002<sup>c</sup></td></tr><tr><td align="center" colspan="1" valign="top">2018</td><td colspan="1" valign="top" align="center">356</td><td colspan="1" valign="top" align="center">0.090±0.002<sup>f</sup></td><td align="center" colspan="1" valign="top">224</td><td align="center" colspan="1" valign="top">0.055±0.003<sup>f</sup></td><td colspan="1" valign="top" align="center">42</td><td valign="top" align="center" colspan="1">0.038±0.008ᵈ</td><td valign="top" align="center" colspan="1">162</td><td align="center" colspan="1" valign="top">0.043±0.002<sup>c</sup></td></tr><tr><td valign="top" align="center" colspan="1">2019</td><td align="center" colspan="1" valign="top">454</td><td valign="top" align="center" colspan="1">0.125±0.002<sup>c</sup></td><td valign="top" align="center" colspan="1">362</td><td align="center" colspan="1" valign="top">0.092±0.002<sup>bc</sup></td><td valign="top" align="center" colspan="1">134</td><td colspan="1" valign="top" align="center">0.080±0.004<sup>c</sup></td><td colspan="1" valign="top" align="center">272</td><td align="center" colspan="1" valign="top">0.068±0.002ᵇ</td></tr><tr><td valign="top" align="center" colspan="1">2020</td><td align="center" colspan="1" valign="top">353</td><td valign="top" align="center" colspan="1">0.123±0.002<sup>c</sup></td><td colspan="1" valign="top" align="center">371</td><td align="center" colspan="1" valign="top">0.086±0.002<sup>cd</sup></td><td align="center" colspan="1" valign="top">201</td><td colspan="1" valign="top" align="center">0.091±0.003<sup>bc</sup></td><td align="center" colspan="1" valign="top">141</td><td valign="top" align="center" colspan="1">0.073±0.003ᵇ</td></tr><tr><td align="center" colspan="1" valign="top">2021</td><td valign="top" align="center" colspan="1">348</td><td align="center" colspan="1" valign="top">0.152±0.002ᵃ</td><td valign="top" align="center" colspan="1">492</td><td valign="top" align="center" colspan="1">0.104±0.002ᵃ</td><td colspan="1" valign="top" align="center">192</td><td align="center" colspan="1" valign="top">0.111±0.004ᵃ</td><td valign="top" align="center" colspan="1">204</td><td valign="top" align="center" colspan="1">0.069±0.002ᵇ</td></tr><tr><td valign="top" align="center" colspan="1">2022</td><td valign="top" align="center" colspan="1">607</td><td align="center" colspan="1" valign="top">0.132±0.001ᵇ</td><td valign="top" align="center" colspan="1">636</td><td colspan="1" valign="top" align="center">0.095±0.002ᵇ</td><td align="center" colspan="1" valign="top">192</td><td align="center" colspan="1" valign="top">0.100±0.004<sup>ab</sup></td><td align="center" colspan="1" valign="top">222</td><td align="center" colspan="1" valign="top">0.086±0.002ᵃ</td></tr><tr><td align="center" colspan="1" valign="top">2023</td><td valign="top" align="center" colspan="1">672</td><td valign="top" align="center" colspan="1">0.148±0.001ᵃ</td><td valign="top" align="center" colspan="1">629</td><td align="center" colspan="1" valign="top">0.110±0.002ᵃ</td><td valign="top" align="center" colspan="1">227</td><td valign="top" align="center" colspan="1">0.107±0.003<sup>ab</sup></td><td valign="top" align="center" colspan="1">177</td><td valign="top" align="center" colspan="1">0.095±0.002ᵃ</td></tr><tr><td align="center" colspan="1" valign="top">2024</td><td align="center" colspan="1" valign="top">514</td><td align="center" colspan="1" valign="top">0.115±0.001ᵈ</td><td colspan="1" valign="top" align="center">363</td><td valign="top" align="center" colspan="1">0.087±0.002<sup>cd</sup></td><td align="center" colspan="1" valign="top">76</td><td align="center" colspan="1" valign="top">0.092±0.006<sup>bc</sup></td><td align="center" colspan="1" valign="top">7</td><td align="center" colspan="1" valign="top">0.042±0.013<sup>c</sup></td></tr></tbody></table><table-wrap-foot><p>Note: ADG3=Average daily gain from 0 to 3-months old, ADG6=Average daily gain from 3 to 6-months old, ADG8=Average daily gain from 6 to 8-months old, ADG12=Average daily gain from 8 to 12-months old. Means in the same column with different superscript differ significantly (*  = p&lt;0.05) or (** = p&lt;0.01).</p></table-wrap-foot></table-wrap></sec><sec><title>Phenotypic and Genetic Correlation</title><p>All traits evaluated in this study showed positive phenotypic and genetic correlation, which ranged from weak to strong. The phenotypic correlation in this study ranged from 0.14 to 0.87, while the genetic correlations ranged from 0.10 to 0.88 (<xref ref-type="fig" rid="figure-ns1ck3">Figure 2</xref>). BW showed weak phenotypic and genetic correlations with other traits, with phenotypic correlation coefficients ranging from 0.14 to 0.25 and genetic correlation coefficients ranging from 0.10 to 0.18. Both phenotypic and genetic correlations increased with the advancing age of the animals. The WW, 6MW, 8MW, and 12MW had strong, positive phenotypic correlations (0.54-0.92) and genetic correlations (0.56-0.88). The strongest correlation was observed between 6MW and 8MW, with a phenotypic correlation of 0.92 and a genetic correlation of 0.88.</p><fig id="figure-ns1ck3" ignoredToc=""><label>Figure 2</label><caption><p> Phenotypic correlation (above diagonal) and genetic correlation (below diagonal) of Etawah Grade (EG) goat. BW=Birth weight, WW=Weaning weight, 6MW= 6-months weight, 8MW=8-months weight, 12MW=12-months weight.</p></caption><graphic mime-subtype="png" mimetype="image" xlink:href="https://journal.ipb.ac.id/tasj/article/download/71513/version/51978/33951/414683"><alt-text>Image</alt-text></graphic></fig><table-wrap id="table-4" ignoredToc=""><label>Table 4</label><caption><p>Estimates of the (co)variance components and the genetic parameters studied for the traits of Etawah Grade (EG) goats</p></caption><table frame="box" rules="all"><thead><tr><th align="left" colspan="1" valign="top">Traits</th><th colspan="1" valign="top" align="center"><inline-formula><tex-math id="math-7"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_a^2 \end{document} ]]></tex-math></inline-formula></th><th valign="top" align="center" colspan="1"><inline-formula><tex-math id="math-8"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_e^2 \end{document} ]]></tex-math></inline-formula></th><th align="center" colspan="1" valign="top"><inline-formula><tex-math id="math-9"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_p^2 \end{document} ]]></tex-math></inline-formula></th><th align="center" colspan="1" valign="top">h²±SE</th></tr></thead><tbody><tr><td align="left" colspan="1" valign="top">BW</td><td valign="top" align="center" colspan="1">0.100</td><td align="center" colspan="1" valign="top">0.217</td><td align="center" colspan="1" valign="top">0.317</td><td valign="top" align="center" colspan="1">0.314±0.028</td></tr><tr><td valign="top" align="left" colspan="1">WW</td><td align="center" colspan="1" valign="top">3.219</td><td align="center" colspan="1" valign="top">8.889</td><td align="center" colspan="1" valign="top">12.108</td><td valign="top" align="center" colspan="1">0.265±0.034</td></tr><tr><td valign="top" align="left" colspan="1">6MW</td><td align="center" colspan="1" valign="top">7.439</td><td valign="top" align="center" colspan="1">13.640</td><td valign="top" align="center" colspan="1">21.079</td><td valign="top" align="center" colspan="1">0.352±0.038</td></tr><tr><td valign="top" align="left" colspan="1">8MW</td><td valign="top" align="center" colspan="1">6.893</td><td valign="top" align="center" colspan="1">18.268</td><td valign="top" align="center" colspan="1">25.161</td><td valign="top" align="center" colspan="1">0.273±0.054</td></tr><tr><td align="left" colspan="1" valign="top">12MW</td><td colspan="1" valign="top" align="center">7.661</td><td align="center" colspan="1" valign="top">22.359</td><td valign="top" align="center" colspan="1">30.020</td><td align="center" colspan="1" valign="top">0.254±0.052</td></tr><tr><td valign="top" align="left" colspan="1">ADG3</td><td valign="top" align="center" colspan="1">0.0004</td><td valign="top" align="center" colspan="1">0.001</td><td valign="top" align="center" colspan="1">0.0014</td><td align="center" colspan="1" valign="top">0.254±0.034</td></tr><tr><td valign="top" align="left" colspan="1">ADG6</td><td valign="top" align="center" colspan="1">0.0002</td><td align="center" colspan="1" valign="top">0.002</td><td colspan="1" valign="top" align="center">0.0022</td><td align="center" colspan="1" valign="top">0.135±0.029</td></tr><tr><td valign="top" align="left" colspan="1">ADG8</td><td align="center" colspan="1" valign="top">0.0004</td><td align="center" colspan="1" valign="top">0.002</td><td align="center" colspan="1" valign="top">0.0024</td><td valign="top" align="center" colspan="1">0.161±0.053</td></tr><tr><td valign="top" align="left" colspan="1">ADG12</td><td valign="top" align="center" colspan="1">0.0001</td><td valign="top" align="center" colspan="1">0.001</td><td valign="top" align="center" colspan="1">0.0011</td><td valign="top" align="center" colspan="1">0.085±0.034</td></tr></tbody></table><table-wrap-foot><p>Note: BW=Birth weight, WW=Weaning weight, 6MW= 6-months weight, 8MW=8-months weight, 12MW=12-months weight, ADG3=Average daily gain from 0 to 3-months old, ADG6=Average daily gain from 3 to 6-months old, ADG8=Average daily gain from 6 to 8-months old, ADG12=Average daily gain from 8 to 12-months old, <inline-formula><tex-math id="math-10"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_a^2 \end{document} ]]></tex-math></inline-formula> = the additive genetic variance of the animal, <inline-formula><tex-math id="math-11"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_e^2 \end{document} ]]></tex-math></inline-formula> = the residual variance, <inline-formula><tex-math id="math-12"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \sigma_p^2 \end{document} ]]></tex-math></inline-formula> = the phenotypic variance, and SE= Standard error.</p></table-wrap-foot></table-wrap></sec><sec><title>Estimated Genetic Trend</title><p>The estimated genetic trend in this study, calcu-lated using Estimated Breeding Values (EBV), indicated increased BW, WW, 6MW, and 12MW by 0.006; 0.048; 0.044; and 0.144 kg year<sup>-1</sup>, respectively, while 8MW declined by -0.006 kg year<sup>-1</sup> (<xref ref-type="table" rid="table-5">Table 5</xref> and <xref ref-type="fig" rid="figure-2"> Figure 3</xref>). Significant genetic trends (p&lt;0.01) were observed for all body weight traits, except for 8MW, which showed a non-significant genetic trend (p&gt;0.05). The genetic trend for BW showed minimal fluctuation, indicating that it remained relatively stable from year to year. In contrast, the genetic trend for WW, 8MW, and 12MW showed a slight decline from 2016 to 2018, then continued to decline, reaching a peak in 2021. A different pattern was observed at 6MW, where the genetic trends showed a relatively stable increase from 2016 to 2024.</p><table-wrap id="table-5" ignoredToc=""><label>Table 5</label><caption><p>Estimated body weight genetic trend of Etawah Grade goat (kg year-¹)</p></caption><table frame="box" rules="all"><thead><tr><th align="center" colspan="1" valign="top">BW</th><th valign="top" align="center" colspan="1">WW</th><th valign="top" align="center" colspan="1">6MW</th><th valign="top" align="center" colspan="1">8MW</th><th valign="top" align="center" colspan="1">12MW</th></tr></thead><tbody><tr><td colspan="1" valign="top" align="center">0.006 ± 0.001**</td><td align="center" colspan="1" valign="top">0.048 ± 0.006**</td><td align="center" colspan="1" valign="top">0.044 ± 0.012**</td><td align="center" colspan="1" valign="top">-0.006 ± 0.019</td><td valign="top" align="center" colspan="1">0.144 ± 0.016**</td></tr></tbody></table><table-wrap-foot><p>Note: BW=Birth weight, WW=Weaning weight, 6MW= 6-months weight, 8MW=8-months weight, 12MW=12-months. ** = p&lt;0.01 level of significance</p></table-wrap-foot></table-wrap><fig id="figure-2" ignoredToc=""><label>Figure 3</label><graphic xlink:href="https://journal.ipb.ac.id/tasj/article/download/71513/version/51978/33951/414684" mime-subtype="png" mimetype="image"><alt-text>Image</alt-text></graphic></fig><p>A similar pattern was observed for average daily gain. The genetic trends for ADG3, ADG6, and ADG12 increased by 0.0004, 0.0002, and 0.0003 kg year-1, respectively, while ADG8 decreased by 0.0003 kg year<sup>-1</sup> (<xref ref-type="table" rid="table-6">Table 6</xref> and <xref rid="figure-3" ref-type="fig">Figure 4</xref>). Highly Significant genetic trends (p&lt;0.01) were observed for every average daily gain, except for ADG8, which showed a significant genetic trend (P&lt;0.05). The genetic trends for average daily gain fluctuated, with ADG3 and ADG8 showing a declining tendency observed from 2021 onward. ADG12 showed a sharp decline between 2023 and 2024. In contrast, the genetic trend for ADG6 remained relatively stable and showed an increasing tendency compared to the other traits.</p><table-wrap id="table-6" ignoredToc=""><label>Table 6</label><caption><p>Estimated average daily gain genetic trend of Etawah Grade goat (kg day-¹ year-¹)</p></caption><table frame="box" rules="all"><thead><tr><th valign="top" align="center" colspan="1">ADG3</th><th valign="top" align="center" colspan="1">ADG6</th><th valign="top" align="center" colspan="1">ADG8</th><th valign="top" align="center" colspan="1">ADG12</th></tr></thead><tbody><tr><td align="center" colspan="1" valign="top">0.0004±0.00007**</td><td align="center" colspan="1" valign="top">0.0002 ± 0.00005**</td><td valign="top" align="center" colspan="1">-0.0003 ± 0.0001*</td><td valign="top" align="center" colspan="1">0.0003± 0.00005**</td></tr></tbody></table><table-wrap-foot><p>Note: ADG3=Average daily gain from 0 to 3-months old, ADG6=Average daily gain from 3 to 6-months old, ADG8=Average daily gain from 6 to 8-months old, ADG12=Average daily gain from 8 to 12-months old. * = p&lt;0.05 and ** = p&lt;0.01 level of significance.</p></table-wrap-foot></table-wrap><fig id="figure-3" ignoredToc=""><label>Figure 4</label><graphic mime-subtype="png" mimetype="image" xlink:href="https://journal.ipb.ac.id/tasj/article/download/71513/version/51978/33951/414685"><alt-text>Image</alt-text></graphic></fig></sec></sec><sec><title>DISCUSSION</title><p>The overall means of BW, WW, 6MW, 8MW, and 12MW observed in this study were 3.491±0.008 kg, 14.754±0.060 kg, 21.223±0.085 kg, 26.062±0.151 kg, and 31.062±0.167 kg, respectively. The BW recorded aligns with previous findings on Turkish Saanen goats<xref ref-type="bibr" rid="BIBR-13">(Erdoğan Ataç et al., 2023)</xref> and exceeds those reported for Inner Mongolia White Cashmere goats<xref ref-type="bibr" rid="BIBR-44">(Shi et al., 2024)</xref> and Boer x Highland goats<xref ref-type="bibr" rid="BIBR-48">(Tesema et al., 2021)</xref>, with values of 3.33, 2.54, and 2.52 kg, respectively. The weaning weight (WW) in the present study was lower than that reported for Turkish Saanen goats<xref ref-type="bibr" rid="BIBR-13">(Erdoğan Ataç et al., 2023)</xref>, with values of 18.38 kg and 15.17 kg for Inner Mongolia White Cashmere goats<xref ref-type="bibr" rid="BIBR-44">(Shi et al., 2024)</xref>, but has a higher value than that of the Assam Hill goat<xref rid="BIBR-43" ref-type="bibr">(Sarma et al., 2019)</xref>. Rout <italic>et al</italic>. (2018)<xref ref-type="bibr" rid="BIBR-40">(Rout et al., 2018)</xref> reported lower 6MW, 8MW, and 12MW values for Jamunapari goats compared to those observed in the present study, with respective values of 14.5, 19.4, and 23.9 kg. Similarly, Magotra <italic>et al</italic>. (2021)<xref rid="BIBR-31" ref-type="bibr">(Magotra et al., 2021)</xref> reported lower 6MW, 8MW, and 12MW body weights in Beetal goats compared to the present study, with values of 13.8, 17.8, and 20.2 kg, respectively. Variations in body weight among goat breeds are primarily determined by genetic potential and breed-specific production objectives. Cashmere-type goat is more adapted for fiber production rather than rapid growth or large body size<xref ref-type="bibr" rid="BIBR-16">(Gawat et al., 2023)</xref>. Small-framed goat breeds are typically found in harsh environments, where their smaller body weight represents a trade-off that enhances reproductive efficiency and environmental adaptability<xref ref-type="bibr" rid="BIBR-3">(Amiri et al., 2023)</xref>. However, dairy-type goats generally have large body sizes, and the males are often utilized for meat production, resulting in relatively high body weight<xref ref-type="bibr" rid="BIBR-16">(Gawat et al., 2023)</xref>.</p><p>The overall mean and standard error values for ADG3, ADG6, ADG8, and ADG12 of the EG goat were 0.124±0.001 kg day<sup>-1</sup>, 0.090±0.001 kg day<sup>-1</sup>, 0.091±0.002 kg day<sup>-1</sup>, and 0.068±0.001 kg day<sup>-1</sup>, respectively. Tesema <italic>et al</italic>. (2021)<xref ref-type="bibr" rid="BIBR-48">(Tesema et al., 2021)</xref> reported lower average daily gain values in crossbred Boer goats, with 0.080 kg day<sup>-1</sup> for ADG3, 0.038 kg day<sup>-1</sup> for ADG6, 0.042 kg day<sup>-1</sup> for ADG8, and 0.030 for ADG12. In contrast, Wang <italic>et al</italic>. (2024b)<xref ref-type="bibr" rid="BIBR-53">(Wang et al., 2024)</xref> reported higher average daily gain values in Dumeng sheep compared to the present study, with ADG3 and ADG6 values of 0.302 kg day<sup>-1</sup> and 0.232 kg day<sup>-1</sup>, respectively. The observed differences in growth traits between the present and previous studies may be attributed to variations in agroclimatic conditions and the genetic backgrounds of the breeds.</p><p>Significant differences (p&lt;0.01) in body weight and average daily gain were observed between male and female goats across all age groups. Male EG goats showed higher body weights and average daily gains than females at every age. These findings are consistent with previous research, which indicated that male goats demonstrated a higher growth rate than female goats<xref ref-type="bibr" rid="BIBR-34">(Markos et al., 2023)</xref>. Phenotypic differences between males and females are referred to as sexual size dimorphism and are primarily attributed to difference in endocrine conditions and associated with nutrient requirements<xref ref-type="bibr" rid="BIBR-17">(Ghafouri-Kesbi &amp; Baneh, 2018)</xref>. Sex hormones influence the growth-related genes, even though males and females share the same genome. Androgen and estrogen hormones are known to have different concentrations between males and females and influence growth traits<xref rid="BIBR-18" ref-type="bibr">(Ghione &amp; Dean, 2025)</xref>. High levels of androgen hormones in male goats enhance muscle development by increasing the protein synthesis rates<xref ref-type="bibr" rid="BIBR-49">(Tesema et al., 2022)</xref>. In contrast, estrogen in females delays growth by restricting long bones’ elongation, resulting in lower body weight compared to males, but supporting earlier sexual maturity<xref ref-type="bibr" rid="BIBR-18">(Ghione &amp; Dean, 2025)</xref>. High estrogen levels in female goats can also reduce dry matter intake, further affecting their growth<xref ref-type="bibr" rid="BIBR-42">(Safdar &amp; Sadeghi, 2015)</xref>. Sexual size dimorphism has important implications for management and breeding strategies, as rapid muscle development in males makes male goats more suitable for meat production.</p><p>Type of birth had a highly significant effect (p&lt;0.01) on all traits, except ADG12, for which no significant effect (p&gt;0.05) was observed. Single-born goats had the highest BW, WW, 6MW, 8MW, ADG3, and ADG6 compared to other birth types. The 12MW showed relatively similar values among all types of birth. Previous studies have also reported lower body weight and slower growth in multiple-born kids in both EG goats<xref ref-type="bibr" rid="BIBR-25">(Husen et al., 2025)</xref> and Boer goats<xref ref-type="bibr" rid="BIBR-54">(Zhang et al., 2009)</xref>. The variation in growth rate among birth types is influenced by intrauterine competition for space and nutrients<xref ref-type="bibr" rid="BIBR-20">(Gootwine, 2020)</xref>. A single-born goat kid would not have to compete to get space and nutrients in the uterus during the embryonic period. Differences in growth and body weight during the weaning period are further influenced by competition for milk from the doe during the suckling period. Limited milk production of doe goats during lactation may result in lower growth rates for multiple-born kids compared to single-born kids<xref ref-type="bibr" rid="BIBR-44">(Shi et al., 2024)</xref>. Lower body weight during the post-weaning period in multiple-born kids may be influenced by a slower growth rate during the suckling period compared with single-born kids<xref ref-type="bibr" rid="BIBR-23">(Hasan et al., 2014)</xref>. After the suckling period, the maternal effect becomes minimal, and the feeding program shifts to free feeding. As animals grow older, their physical fitness continues to improve, and their immunity gradually strengthens<xref ref-type="bibr" rid="BIBR-44">(Shi et al., 2024)</xref>. This effect allowed goats with multiple-birth types to achieve similar or even faster growth rates compared to single-born kids.</p><p>Year of birth had a highly significant (p&lt;0.01) effect for all traits, although the trend fluctuated across years (<xref ref-type="table" rid="table-2">Table 2</xref>). BW remained relatively stable from 2015 to 2024, ranging from 3.37 to 3.59 kg, with the lowest BW being reached in 2019 and the highest in 2020. The lowest WW, 6MW, 8MW, and 12MW, were observed for goats born in 2018, while the highest WW was observed in 2021 with the value of 17.37 kg. The highest trend of 6MW, 8MW, and 12MW was observed in 2023 with values of 24.34, 28.77, and 39.04 kg, respectively. The lowest of ADG3, ADG6, ADG8 was in 2018 with the value of 0.090±0.002 kg day<sup>-1</sup>, 0.055±0.003 kg day<sup>-1</sup>, and 0.038±0.008 kg day<sup>-1</sup>, respectively. The highest value of ADG3 (0.152±0.002 kg day<sup>-1</sup>) and ADG8 (0.111±0.004 kg day<sup>-1</sup>) were reached in 2021, while the highest ADG6 was observed in 2023 with the value of 0.110±0.002 kg day<sup>-1</sup>. The highest ADG12 was reached in 2023 (0.095±0.002 kg day<sup>-1</sup>) and the lowest in 2024 (0.042±0.013 day<sup>-1</sup>). The variation in body weight and growth rate across years is attributed to climate change, which affected feed availability during those years<xref ref-type="bibr" rid="BIBR-35">(Menezes et al., 2016)</xref>. The differences in goat growth traits across years were also influenced by the management practices implemented in each respective year, including health management and feeding management<xref ref-type="bibr" rid="BIBR-23">(Hasan et al., 2014)</xref>.</p><p>BW, WW, 6MW, 12MW, ADG3, ADG6, and ADG12 were significantly affected by season of birth (p&lt;0.01), while 8MW and ADG8 were not significantly affected (p&gt;0.05). Goats born in the rainy season showed higher body weight and average daily gain in early growth traits (BW, WW, and 6MW) compared to those born in the dry season. On the contrary, goats born in the dry season showed better performance in later growth traits (8MW and 12MW). Abebe <italic>et al</italic>. (2023)<xref rid="BIBR-1" ref-type="bibr">(Abebe et al., 2023)</xref> reported a similar result that BW, WW, and 6MW of lambs born in the rainy seasons were heavier than those born in the dry season. Early growth traits, particularly BW and WW, are largely determined by the dam’s nutritional intake. During the rainy season, vegetation is more varied and nutritious than in the dry season. Lo <italic>et al</italic>. (2024)<xref rid="BIBR-30" ref-type="bibr">(Lo et al., 2024)</xref> noted that the crude protein content of the forage during the rainy season is higher than during the dry season, whereas the dry matter content during the dry season was higher than during the rainy season. Better feed availability and nutritional quality during the rainy season are associated with endocrine conditions in dams, particularly increased prolactin secretion and milk production, thereby contributing to higher weaning weights<xref ref-type="bibr" rid="BIBR-14">(Farrag, 2022)</xref>. Elevated insulin levels during the rainy season stimulate anabolic processes in muscle and liver tissues, improving carbohydrate and lipid metabolism<xref ref-type="bibr" rid="BIBR-36">(Murillo-Ortiz et al., 2013)</xref>;<xref ref-type="bibr" rid="BIBR-46">(Song et al., 2025)</xref>. These metabolic effects contribute to improved post-weaning growth and are positively associated with increased neonatal birth weight through enhanced maternal nutrient utilization<xref ref-type="bibr" rid="BIBR-46">(Song et al., 2025)</xref>. In later growth phases, growth is more influenced by dry matter intake, organic matter intake, and energy supply<xref ref-type="bibr" rid="BIBR-52">(Wang et al., 2024)</xref>. This phenomenon explains the higher BW, WW, and 6MW in goats born during the rainy season, while 12MW is higher in those born during the dry season. Higher body weight at 12MW during the dry season may result from compensatory growth after nutritional restriction, increased feed intake under low-quality forage conditions, and improved nutrient utilization efficiency during post-weaning growth.</p><p>Parity had a highly significant (p&lt;0.01) effect on BW, WW, 6MW, 8MW, 12MW, and ADG3, a significant effect (p&lt;0.05) on ADG6, and no effect (p&gt;0.05) on ADG8 and ADG12. The highest BW was observed in offspring from second or third parity dams, while the lowest values were recorded in offspring from first parity dams. WW, 6MW, 8MW, and 12MW were the highest in offspring from first-parity dams, with body weight decreasing gradually with the increase in parity. ADG3 and ADG6 showed a gradual decrease as the number of parities increased. Parity of dams influences kid performance due to the development of the dam’s uterus with increasing age and frequency of parturition<xref ref-type="bibr" rid="BIBR-23">(Hasan et al., 2014)</xref>. Similar effects of parity on body weight have been reported in previous studies<xref ref-type="bibr" rid="BIBR-12">(Ehsaninia, 2021)</xref>. Multiparous dams tend to produce larger litter size compared to primiparous dams<xref ref-type="bibr" rid="BIBR-32">(Mamutse et al., 2023)</xref>. There is an antagonistic relationship between body weight and litter size, particularly during early growth stages<xref ref-type="bibr" rid="BIBR-6">(Besufkad et al., 2024)</xref>, which may explain the higher BW, WW, 6MW, and 8MW in offspring from primiparous dams compared to those from multiparous dams. Early growth of the goat is strongly affected by maternal influences, since the nutrient availability depends primarily on the dam’s nutritional status during the prenatal period. However, maternal effects gradually decline as offspring age.</p><p>The heritability of BW, WW, 6MW, 8MW, and 12MW were estimated at 0.314±0.028, 0.265±0.034, 0.352±0.038, 0.273±0.054, and 0.254±0.052, respectively. Heritability values above 0.4 are classified as high heritability, 0.2 to 0.4 as medium heritability, and below 0.2 as low heritability<xref ref-type="bibr" rid="BIBR-26">(Jonker et al., 2018)</xref>. Overall, the estimated heritability in this study was classified as moderate. Previous studies reported a higher heritability in West African Dwarf goat of BW (0.45), WW (0.57), 8MW (0.74), 12MW (0.49) than this study, except for 6MW (0.04)<xref ref-type="bibr" rid="BIBR-37">(Ofori &amp; Hagan, 2020)</xref>. In contrast, lower heritability estimates were found in Beetal goats for BW (0.07), 8MW (0.17), and 12MW (0.10), with a similar heritability value for WW (0.27) and a higher value for 6MW (0.37)<xref ref-type="bibr" rid="BIBR-31">(Magotra et al., 2021)</xref>. The estimated heritability of average daily gain traits was low to moderate, ranging from 0.085 to 0.254, and decreased gradually with increasing animal age. Magotra <italic>et al</italic>. (2021)<xref ref-type="bibr" rid="BIBR-31">(Magotra et al., 2021)</xref> reported a similar pattern and lower heritability values for average daily gain in Beetal goats, with 0.21 for ADG3, 0.21 for ADG6, and 0.07 for ADG6. Higher heritability for ADG3 (0.31) was reported in Boer goats<xref ref-type="bibr" rid="BIBR-35">(Menezes et al., 2016)</xref> and Cashmere goats<xref ref-type="bibr" rid="BIBR-51">(Wang et al., 2022)</xref>. Rout <italic>et al</italic>. (2018)<xref ref-type="bibr" rid="BIBR-40">(Rout et al., 2018)</xref> found higher heritability for ADG6 and ADG12, at 0.37 and 0.17, respectively.</p><p>The differences in heritability estimates were due to goat breed and the evaluation methods used<xref ref-type="bibr" rid="BIBR-29">(Ladeira et al., 2021)</xref>. Differences in estimating heritability may also be influenced by sample size and the fixed effects included in the model. Previous studies on the same breed reported higher heritability estimates than those found in the present study. Hasan <italic>et al</italic>. (2014)<xref ref-type="bibr" rid="BIBR-23">(Hasan et al., 2014)</xref> used a smaller sample size and did not account for non-genetic factors as fixed effects. A larger sample size can comprehensively capture variation, making the estimated value more accurate, higher precision, and stronger statistical power, thereby facilitating the discovery of genetic laws<xref ref-type="bibr" rid="BIBR-45">(Shi et al., 2025)</xref>. Non-genetic factors such as gender, breed, dam age, season, year, and type of birth significantly influence determining trait variations and should always be taken into account as fixed effects<xref ref-type="bibr" rid="BIBR-53">(Wang et al., 2024)</xref>.</p><p>Body weight traits showed higher heritability than average daily gain, indicating that environmental variation has a greater impact on average daily gain than on body weight. Higher heritability estimates indicate that body weight traits are more reliable selection criteria than average daily gain in EG goats. Among the traits, 6MW had the highest heritability and can be considered a suitable selection criterion at the early growth stage of EG goats, as it demonstrates the greatest potential to be passed on to the next generation. High heritability estimation indicates that the variation in that trait is mainly influenced by genetic factors rather than environmental factors<xref ref-type="bibr" rid="BIBR-15">(Fathoni et al., 2022)</xref>. Selecting for 6MW can yield higher genetic gain and faster phenotypic improvement compared to other traits. The low estimates of heritability for some traits may suggest that genetic variation is probably unobservable due to environmental factors<xref ref-type="bibr" rid="BIBR-40">(Rout et al., 2018)</xref>. Manirakiza <italic>et al</italic>. (2020)<xref ref-type="bibr" rid="BIBR-33">(Manirakiza et al., 2020)</xref> reported that improvement in traits with low heritability can be achieved through improved recording systems and better management practices, including feeding and health management. Maternal effect also significantly influences the expression of early growth traits; however, their influence decreases as the animal ages<xref ref-type="bibr" rid="BIBR-25">(Husen et al., 2025)</xref>;<xref ref-type="bibr" rid="BIBR-33">(Manirakiza et al., 2020)</xref>. Furthermore, accounting for both maternal genetic and environmental effects is important to improve the accuracy of genetic parameter estimation in future studies.</p><p>The phenotypic and genetic correlations among BW, WW, 6MW, 8MW, and 12MW in this study ranged from weak to strongly positive. Besufkad <italic>et al</italic>. (2024)<xref ref-type="bibr" rid="BIBR-6">(Besufkad et al., 2024)</xref> reported similar findings to this study, with BW showing positive but low phenotypic (0.21-0.28) and genetic correlations (0.20-0.24) with WW, 6MW, and 12MW. A Higher phenotypic and genetic correlation between WW – 6MW, WW – 8MW, and WW–12MW was reported on West African Dwarf goats with values between 0.81-0.92 for phenotypic correlation and 0.75-0.92 for genetic correlation<xref ref-type="bibr" rid="BIBR-37">(Ofori &amp; Hagan, 2020)</xref>. Tesema <italic>et al</italic>. (2021)<xref ref-type="bibr" rid="BIBR-48">(Tesema et al., 2021)</xref> also reported high positive correlations between 6MW and 8MW (0.79) and between 6MW and 12MW (0.71). Positive genetic correlations among the observed traits indicate that these traits are influenced by genes that control more than one trait (pleiotropy)<xref ref-type="bibr" rid="BIBR-22">(Habtegiorgis et al., 2022)</xref>. The positive genetic correlations across all traits in this study indicate that selection for any trait should result in positive genetic change in the others. Indirect selection can also be applied to traits with strong genetic correlations, particularly for traits that are difficult to measure<xref ref-type="bibr" rid="BIBR-7">(Bourdon, 2014)</xref>. Among the evaluated traits, 6MW is the most promising selection criterion for growth in EG goats, as its high heritability and strong genetic correlations are expected to achieve greater genetic improvement in other traits.</p><p>The estimated genetic trends in this study indicated improvements in all evaluated traits, except for 8MW and ADG8. Rout <italic>et al</italic>. (2018)<xref ref-type="bibr" rid="BIBR-40">(Rout et al., 2018)</xref> reported higher estimated genetic trends for BW, WW, 6MW, 8MW, and 12MW in Jamunapari goats, with values of 0.037, 0.080, 0.118, 0.144, and 0.199 kg year<sup>-1</sup>, respectively. In contrast, Tesema <italic>et al</italic>. (2021)<xref ref-type="bibr" rid="BIBR-48">(Tesema et al., 2021)</xref> observed declines in genetic trends for BW, WW, and 6MW in Boer x Highland goats, with values of 0.0207, 0.0805, and 0.0317 kg year<sup>-1</sup>, while 8MW and 12MW increased by 0.1692 and 0.2133 kg year<sup>-1</sup>, respectively. Ren <italic>et al</italic>. (2024)<xref ref-type="bibr" rid="BIBR-38">(Ren et al., 2024)</xref> reported higher genetic trends for ADG3 but lower genetic trends for ADG6 in Luzhong sheep, at 0.0012 kg day<sup>-1</sup> and 0.00002 kg day<sup>-1</sup>, respectively. Low estimated genetic trends may be attributed to climatic conditions that reduced feed availability and decreased livestock productivity in the observed year<xref ref-type="bibr" rid="BIBR-22">(Habtegiorgis et al., 2022)</xref>. The positive and significant genetic trends observed for BW, WW, 6MW, 12MW, ADG3, ADG6, and ADG12 indicate that the selection program implemented at the breeding station has been effective in improving these traits genetically over the years. However, these trends observed were lower than those reported in previous studies across several goat breeds. The low estimated genetic trend suggests that the selection program implemented at the breeding station in recent years has not been fully effective in achieving optimal genetic improvement. The low estimated genetic trend indicates that the selection differential was not maximized; other factors contributing to the low genetic trend include selection practices that do not account for estimated breeding values and the culling of animals with low productivity at specific ages<xref ref-type="bibr" rid="BIBR-48">(Tesema et al., 2021)</xref>;<xref ref-type="bibr" rid="BIBR-19">(Gholizadeh &amp; Ghafouri-Kesbi, 2015)</xref>. Several strategies that can be implemented to enhance genetic trends include reducing the generation interval and increasing selection intensity<xref ref-type="bibr" rid="BIBR-24">(He et al., 2023)</xref>;<xref ref-type="bibr" rid="BIBR-27">(Kasinathan et al., 2015)</xref>. The most practical approach to reducing the generation interval is to shorten the length of sire usage and to implement reproductive technologies such as artificial insemination (AI). The application of genomic selection has also been proven to reduce the generation interval, as replacement animals can be selected at a relatively young age<xref ref-type="bibr" rid="BIBR-8">(Roos et al., 2011)</xref>.</p><p>These findings emphasize the need to account for non-genetic variation when estimating genetic parameters for selection programs in EG goat populations. Adjusting body weight for non-genetic factors will reduce bias in estimating genetic parameters. In future studies, both maternal genetic and maternal environmental effects should be considered in the estimation of genetic parameters to increase the accuracy of the estimates, especially for early growth traits. The findings of this study may provide a basis for decision-making in production management to prevent performance decline driven by the effects of non-genetic factors. Several strategies, including management improvement and implementation of technology, are required to enhance the genetic trend for growth traits in EG goats.</p></sec><sec><title>CONCLUSION</title><p>Growth traits in EG goats are significantly influenced by several non-genetic factors, including sex, birth type, year of birth, season, and parity. Notably, only 8MW was unaffected by the season of birth. The estimated heritability of growth traits in EG goats was moderate, suggesting sufficient genetic variability to respond to selection. Among the evaluated traits, 6MW exhibited the highest heritability and strong genetic associations with later growth traits; it could serve as an effective selection criterion in EG goat breeding programs. A positive genetic correlation among growth traits suggests that improvement in one trait may lead to favorable responses in related traits. The negative genetic trend may indicate inconsistencies in selection practices or management conditions during the study period.</p></sec></body><back><ack><sec><title>ACKNOWLEDGEMENT</title><p>The authors are grateful to the Ministry of Finance of Indonesia for supporting this research through the Lembaga Pengelola Dana Pendidikan (LPDP) Program under contract number LOG-21191/LPDP.3/2024 (contract year: 2024). Appreciation is also extended to the National Breeding Station of Pelaihari, Ministry of Agriculture of Indonesia, for assistance in data collection and provision.</p></sec></ack><sec><title>DECLARATION OF GENERATIVE AI AND AI-ASSISTED TECHNOLOGIES IN THE WRITING PROCESS</title><p>During the preparation of this work, the authors used ChatGPT and Grammarly in order to improve the readability and language of the work. 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