TABLE 2.
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 | HF | Candidate genes within this QTL | ||
Angus | 8 | 19919026 | 20930648 | 3 | 20426751b | 4.18 × 10–6 | 0.057 | 0.980 | 0.014 | 0.896 | 0.112 | 0.989 | ELAVL2* |
10 | 101530896 | 102548539 | 4 | 102040999b | 5.32 × 10–7 | 0.232 | 0.678 | 0.305 | 0.306 | 0.216 | 0.223 | TTC8, FOXN3* | |
11 | 52112729 | 53133828 | 13 | 52632756a | 1.85 × 10–6 | 0.639 | 0.241 | 0.895 | 0.908 | 0.898 | 0.105 | ||
12 | 12006341 | 13006349 | 2 | 12506341a | 2.69 × 10–8 | 0.073 | 0.047 | 0.943 | 0.000 | 0.918 | 0.963 | VWA8, DGKH, TNFSF11, AKIP11 | |
28 | 2715813 | 4028680 | 11 | 3522966d | 1.14 × 10–6 | 0.832 | 0.806 | 0.201 | 0.000 | 0.808 | 0.220 | SPRTN, TRIM67* | |
Charolais | 3 | 75099566 | 76200376 | 43 | 75636445b | 2.40 × 10–7 | 0.111 | 0.071 | 0.000 | 0.000 | 0.903 | 0.168 | CTH, LRRC7*, LRRC40 |
9 | 12560255 | 13754168 | 9 | 13060255a | 3.52 × 10–7 | 0.990 | 0.016 | 0.991 | 0.985 | 0.987 | 0.000 | MTO1, EEF1A1 | |
10 | 42104985 | 43116388 | 3 | 42604985a | 3.68 × 10–7 | 0.003 | 0.039 | 0.992 | 0.948 | 0.030 | 0.991 | RPL36AL, MGAT2, ARF6, SOS2 | |
11 | 10962219 | 12944023 | 11 | 11462219b | 3.04 × 10–7 | 0.000 | 0.007 | 0.000 | 0.000 | 0.000 | 0.000 | ALMS1, EGR4, SMYD5, CYP26B1, SFXN5* | |
18 | 57584619 | 58600780 | 3 | 58084619d | 1.61 × 10–7 | 0.002 | 0.012 | 0.991 | 0.004 | 0.031 | 0.000 | ENSBTAG00000014593* | |
Hereford | 4 | 82061233 | 83396596 | 4 | 82561233a | 2.12 × 10–7 | 0.000 | 0.989 | 0.023 | 0.012 | 0.994 | 0.993 | POU6F2 |
6 | 38955125 | 39995325 | 14 | 39461621a | 6.63 × 10–7 | 0.308 | 0.000 | 0.852 | 0.000 | 0.000 | 0.604 | LCORL | |
7 | 79663134 | 80729587 | 3 | 80197062a | 8.60 × 10–9 | 0.013 | 0.014 | 0.996 | 0.000 | 0.012 | 0.978 | ||
10 | 56443792 | 57546809 | 7 | 57025496a | 9.84 × 10–8 | 0.961 | 0.000 | 0.967 | 0.050 | 0.893 | 0.062 | WDR72 | |
23 | 8222426 | 9377363 | 9 | 8722426d | 1.37 × 10–7 | 0.010 | 0.009 | 0.005 | 0.005 | 0.010 | 0.979 | UHRF1BP1*, HMGA1, NUDT3, SCUBE3 | |
Limousin | 1 | 61741512 | 63549298 | 3 | 63048403a | 1.08 × 10–6 | 0.439 | 0.000 | 0.650 | 0.730 | 0.449 | 0.225 | |
6 | 37530341 | 38792617 | 34 | 38284104b | 1.09 × 10–7 | 0.298 | 0.000 | 0.685 | 0.565 | 0.722 | 0.460 | PPM1K, ABCG2*, PKD2*, SPP1, MEPE*, LAP3 | |
18 | 9391406 | 10382598 | 13 | 9891406b | 1.69 × 10–6 | 0.211 | 0.249 | 0.109 | 0.137 | 0.447 | 0.136 | CDH13*, HSBP1, MLYCD | |
18 | 55221720 | 56247875 | 3 | 55721720d | 1.39 × 10–6 | 0.995 | 0.000 | 0.002 | 0.003 | 0.000 | 0.000 | LIG1, KCNJ14, CYTH2, RPL18, PPP1R15A | |
20 | 7457546 | 8466248 | 16 | 7959103a | 9.82 × 10–7 | 0.057 | 0.008 | 0.990 | 0.987 | 0.979 | 0.000 | UTP15, ANKRA2 | |
Simmental | 13 | 70061402 | 71118226 | 7 | 70573855a | 2.82 × 10–6 | 0.010 | 0.050 | 0.987 | 0.897 | 0.055 | 0.998 | TOP1, PLCG1, LPIN3 |
23 | 10151181 | 11174475 | 3 | 10651181b | 1.20 × 10–6 | 0.071 | 0.913 | 0.054 | 0.128 | 0.068 | 0.959 | CPNE5*, PIM1, TMEM217, TBC1D22B | |
23 | 30033517 | 31047355 | 4 | 30533517c | 1.67 × 10–6 | 0.099 | 0.072 | 0.219 | 0.187 | 0.902 | 0.146 | ZSCAN31, ZKSCAN4, HIST1H2BB | |
25 | 8699062 | 9699134 | 5 | 9199062a | 6.83 × 10–7 | 0.000 | 0.000 | 0.996 | 0.000 | 0.005 | 0.996 | EMP2, NUBP1, CLEC16A | |
26 | 48445354 | 49451650 | 6 | 48945354a | 2.03 × 10–6 | 0.989 | 0.008 | 0.996 | 0.041 | 0.996 | 0.000 | ||
Holstein Friesian | 1 | 57000435 | 58139976 | 15 | 57582901b | 7.42 × 10–7 | 0.034 | 0.225 | 0.209 | 0.688 | 0.000 | 0.195 | ABHD10, CD200*, ATG3, CCDC80 |
2 | 30344158 | 31344250 | 3 | 30844250a | 7.56 × 10–7 | 0.003 | 0.000 | 0.994 | 0.987 | 0.998 | 0.990 | TTC21B, GALNT3, CSRNP3 | |
10 | 39919494 | 41220895 | 5 | 40476976a | 1.04 × 10–6 | 0.004 | 0.004 | 0.975 | 0.991 | 0.982 | 0.861 | MDGA3* | |
13 | 78475631 | 79544490 | 9 | 79027846a | 9.15 × 10–7 | 0.059 | 0.098 | 0.045 | 0.765 | 0.840 | 0.073 | SNAI1, UBE2V1, PTPN1 | |
24 | 827290 | 2268995 | 9 | 1331600a | 4.86 × 10–7 | 0.064 | 0.067 | 0.986 | 0.000 | 0.924 | 0.013 | PQLC1, KCNG2, NFATC1, ATP9B |
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.