<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Arzik Y</submitter><funding>Bilimsel Araştırma Projeleri, Erciyes Üniversitesi</funding><pagination>18477</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9630504</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>The aim of this study was to estimate genomic heritability and the impact that genetic backgrounds have on blood parameters in Akkaraman sheep by conducting genome-wide association studies and regional heritability mapping analysis. Genomic heritability estimates for blood parameters ranged from 0.00 to 0.55, indicating that measured phenotypes have a low to moderate heritability. A total of 7 genome- and 13 chromosome-wide significant SNPs were associated with phenotypic changes in 15 blood parameters tested. Accordingly, SCN7A, SCN9A, MYADM-like, CCDC67, ITGA9, MGAT5, SLC19A1, AMPH, NTRK2, MSRA, SLC35F3, SIRT6, CREB3L3, and NAV3 genes as well as three undefined regions (LOC101117887, LOC106991526 and LOC105608461) were suggested as candidates. Most of the identified genes were involved i</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Estimates of genomic heritability and genome-wide association studies for blood parameters in Akkaraman sheep.</pubmed_title><pmcid>PMC9630504</pmcid><funding_grant_id>FDK-2020-10807</funding_grant_id><pubmed_authors>Piel LMW</pubmed_authors><pubmed_authors>Arzik Y</pubmed_authors><pubmed_authors>Cinar MU</pubmed_authors><pubmed_authors>Kizilaslan M</pubmed_authors><pubmed_authors>White SN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Estimates of genomic heritability and genome-wide association studies for blood parameters in Akkaraman sheep.</name><description>The aim of this study was to estimate genomic heritability and the impact that genetic backgrounds have on blood parameters in Akkaraman sheep by conducting genome-wide association studies and regional heritability mapping analysis. Genomic heritability estimates for blood parameters ranged from 0.00 to 0.55, indicating that measured phenotypes have a low to moderate heritability. A total of 7 genome- and 13 chromosome-wide significant SNPs were associated with phenotypic changes in 15 blood parameters tested. Accordingly, SCN7A, SCN9A, MYADM-like, CCDC67, ITGA9, MGAT5, SLC19A1, AMPH, NTRK2, MSRA, SLC35F3, SIRT6, CREB3L3, and NAV3 genes as well as three undefined regions (LOC101117887, LOC106991526 and LOC105608461) were suggested as candidates. Most of the identified genes were involved i</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-19T06:18:59.871Z</modification><creation>2025-02-19T00:31:32.914Z</creation></dates><accession>S-EPMC9630504</accession><cross_references><pubmed>36323871</pubmed><doi>10.1038/s41598-022-22966-8</doi></cross_references></HashMap>