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. 2018 Apr 16;96(6):2074–2085. doi: 10.1093/jas/sky131

Table 2.

Phenotypic variance explained by SNP windows for the change in TR during heat stress prior to puberty (prepubertal ΔTR)

SSCa Position start (bp)b Position end (bp)c Variance explained (%)d Candidate gene(s)e
5 69383487 69487000 0.049 TSPAN9, TEAD4
5 72245513 72424166 0.043 MICAL3, LOC102162673
5 69487000 69597659 0.041 TULP3, LOC102162709, ITFG2, LOC102164154
14 136702381 136891524 0.040 ATRNL1, LOC102161079
14 13443000 13564731 0.040 FZD3
5 69437477 69555670 0.039 TEAD4, TULP3, LOC102162709
14 39275817 39773984 0.038
5 69333042 69437477 0.038 TSPAN9, TEAD4
5 72352991 72500090 0.037 LOC102162673
14 139721921 139813511 0.037
5 72141748 72352991 0.036 BID, MICAL3
5 69555670 69691307 0.035 LOC102162709, ITFG2, LOC10216415, LOC102164154, LOC106510369, LOC100512907
14 13564731 13666604 0.035 LOC102157783, EXTL3
14 136824061 136939847 0.035 ATRNL1
14 13356571 13497286 0.034 FBXO16, FZD3
18 27560376 27761494 0.033 ING3, TSPAN12
14 39616077 39904195 0.033 LOC102157597
14 13497286 13621432 0.033 FZD3
1 283482216 283609728 0.032 SUSD1
7 111019262 111170076 0.032
14 136939847 137099653 0.032 ATRNL1
5 70488420 70775116 0.032 ERC1, RAD52
13 215584218 215697149 0.031 C2CD2, LOC102161849
5 69597659 69759629 0.031 LOC102164154, LOC106510369, LOC100512907, IQSEC3

Gene abbreviations: TSPAN9 = tetraspanin 9; TEAD4 = TEA domain transcription factor 4; MICAL3 = microtubule associated monooxygenase, calponin and LIM domain containing 3; ITFG2 = integrin alpha FG-GAP repeat containing 2; EXTL3 = exostosin like glycosyltransferase 3; ATRNL1 = attractin-like 1; FBXO16 = F-box protein 16; FZD3 = frizzled class receptor 3; ING3 = inhibitor of growth family member 3; TSPAN12 = tetraspanin 12; SUSD1 = sushi domain containing 1; ERC1 = ELKS/RAB6-interacting/CAST family member 1; RAD52 = RAD52 homolog, DNA repair protein; C2CD2 = C2 calcium dependent domain containing 2; IQSEC3 = IQ motif and Sec7 domain 3.

aChromosome number of the pig genome for which the SNP window location is mapped.

bSNP window positions start location on the chromosome.

cSNP window position end location on the chromosome.

dPercentage of variance explained by five SNP windows.

eGenes located within the SNP window.