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. 2020 Feb 4;11:20. doi: 10.3389/fgene.2020.00020

TABLE 4.

The location of the most significant QTLs, limited to the top 5, which were associated with back length, and the genes located within these QTLs within each breed.

No of suggestive and significant SNPs Most significant SNP Allele frequency of positive allele

Breed Chr Start End P-Value AA CH HE LM SI Candidate genes within this QTL
Angus 6 37939769 40455422 70 38443019a 5.79 × 10–7 0.139 0.000 0.847 0.207 0.311 PKD2, SPP1, MEPE, LAP3, NCAPG*, LCORL*
6 40762050 42494936 24 41262050b 8.44 × 10–7 0.032 0.003 0.000 0.000 0.000 SLIT2*, PACRGL, KCNIP4*
9 11789073 12803143 4 12298383a 1.17 × 10–6 0.008 0.032 0.979 0.987 0.969 RIMS1, KCNQ5
12 84208854 85283107 29 84720853a 6.13 × 10–8 0.949 0.000 0.013 0.035 0.981
13 68993173 70000878 3 69495192a 6.75 × 10–7 0.026 0.000 0.032 0.073 0.060
Charolais 2 1 10036842 5525 6808074a 3.96 × 10–48 0.000 0.079 0.000 0.972 0.996 WDR75, ASNSD1, ARHGEF4, MYO7B, NAB1, MFSD6, MSTN, PMS1, ORMDL1, COL3A1, COL5A2, ANKAR, SLC40A1
14 33353270 34356964 4 33853270a 1.19 × 10–7 0.000 0.013 0.000 0.000 0.992 ARFGEF1, CPA6, PREX2
14 44425358 45430890 3 44928243a 7.51 × 10–7 0.209 0.273 0.605 0.423 0.423 STMN2, HEY1, MRPS28
28 19217733 21371343 36 19836248a 1.01 × 10–7 0.418 0.784 0.575 0.583 0.626 NRBF2, REEP3*
28 30350477 31864396 38 31332353a 6.88 × 10–9 0.450 0.859 0.629 0.426 0.629 KAT6B*, DUPD1, DUSP13, VDAC2
Hereford 4 1 910718 5 223774a 1.15 × 10–6 0.975 0.984 0.981 0.981 0.000 VSTM2A*
4 37522586 38567213 13 38055263a 2.31 × 10–6 0.959 0.283 0.130 0.851 0.201 PCLO*
8 85462715 87578203 16 86646431a 1.63 × 10–6 0.000 0.000 0.998 0.000 0.000 OGN, ASPN, ECM2, IPPK, BICD2, FGD3, NINJ1, BARX1*,PTPDC1*
14 30747311 31758061 7 31247311a 3.41 × 10–6 0.429 0.333 0.485 0.636 0.648 BHLHE22, MTFR1
18 29621954 30630622 5 30130622a 8.58 × 10–7 0.996 0.995 0.996 0.985 0.010 CDH8
Limousin 1 66063243 67175049 15 66587440b 2.16 × 10–7 0.002 0.030 0.983 0.997 0.018 GTF2E1, STXBP5L, POLQ*, FBXO40, HCLS1, GOLGB1
3 24752329 26688150 3 26188150d 9.48 × 10–7 0.000 0.897 0.908 0.917 0.888 SPAG17*, WDR3, MAN1A2, VTCN1*, TRIM45, TTF2, CD101, PTGFRN
6 32025422 34384319 1058 33661101a 5.14 × 10–13 0.753 0.904 0.407 0.142 0.259 ATOH1
6 36996616 41253691 469 38792702b 4.24 × 10–13 0.097 0.000 0.105 0.091 0.000 ABCG2, PKD2, SPP1*, MEPE, LAP3, NCAPG, LCORL, SLIT2
21 33476048 34502357 6 33999605a 1.55 × 10–6 0.006 0.017 0.005 0.017 0.005 CSPG4, SNX33, IMP3, PTPN9
Simmental 15 77047714 78087312 9 77558153b 5.09 × 10–7 0.811 0.000 0.270 0.000 0.264 DGKZ, ATG13, ARHGAP1, ZNF408, CKAP5*
16 10050545 11308116 5 10550545a 6.88 × 10–7 0.000 0.000 0.000 0.000 0.981
17 62751558 63784022 12 63254862b 1.24 × 10–6 0.047 0.940 0.977 0.930 0.969 LHX5*, PLDB2, OAS2, OAS1Y, OAS1X
20 43798108 44854685 5 44298108a 2.56 × 10–6 0.042 0.069 0.240 0.074 0.109
21 10803227 11841095 7 11303227a 2.88 × 10–6 0.998 0.012 0.980 0.006 0.994 NR2F2

AA, Angus; CH, Charolais; HE, Hereford; LM, Limousin; SE, Simmental; HF, Holstein-Friesian. Superscript denotes SNP classification:aintergenic, bintron, cupstream gene variant, ddownstream gene variant. Symbols denote the significance of SNPs within genes: * gene contained at least one suggestive (p ≤ 1 × 10–5) SNP gene contained at least one significant (p ≤ 1 × 10–8) SNP.