Table 7.
Boundaries of the validated regions with significant dominance effect on calving interval and the most significant SNPs with their associated genes within these regions in discovery and validation populations
Most strongly associated SNP in discovery | Most strongly associated SNP in validation | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
BTCa | Interval (Mbp)b | SNP | Position (bp) | -log10 (P) | Effect ± SE | MAFc | (%)d | SNP | Position (bp) | -log10 (P) | Effect ± SE | MAF | (%) | Genese |
1 | 19.667 - 19.777 | rs110080440 | 19706636 | 4.651 | −3.802 ± 0.896 | 0.299 | 0.091 | rs109600947 | 19776964 | 2.178 | −4.129 ± 1.52 | 0.249 | 0.080 | NA |
2 | 80.202 - 80.654 | rs41591067 | 80201648 | 4.412 | 3.07 ± 0.746 | 0.500 | 0.084 | rs133868000 | 80276795 | 2.403 | −3.268 ± 1.133 | 0.473 | 0.089 | MYO1B f |
3 | 15.808 - 15.963 | rs134910746 | 15947344 | 4.119 | 3.024 ± 0.764 | 0.420 | 0.078 | rs29020504 | 15808470 | 2.505 | −5.434 ± 1.837 | 0.197 | 0.099 | KCNN3 |
7 | 62.509 - 62.852 | rs29013244 | 62508803 | 4.252 | 3.012 ± 0.747 | 0.480 | 0.081 | rs43520270 | 62851917 | 2.123 | 3.664 ± 1.37 | 0.304 | 0.081 | ABLIM3 |
23 | 46.082 - 46.581 | rs137262994 | 46579868 | 4.494 | −3.234 ± 0.777 | 0.407 | 0.087 | rs109881533 | 46081778 | 2.401 | 4.222 ± 1.464 | 0.264 | 0.090 | OFCC1 |
23 | 50.929 - 51.326 | rs110165999 | 51326222 | 5.087 | −5.153 ± 1.154 | 0.205 | 0.101 | rs134147379 | 51081072 | 2.212 | −3.689 ± 1.345 | 0.309 | 0.083 | GMDS |
25 | 39.070 - 39.921 | rs135893130 | 39548382 | 4.364 | −3.225 ± 0.788 | 0.390 | 0.084 | rs108968775 | 39070284 | 2.808 | 3.583 ± 1.131 | 0.489 | 0.108 | LOC618542 |
28 | 43.832 - 44.145 | rs133899460 | 44144815 | 4.032 | −2.918 ± 0.7461 | 0.480 | 0.076 | rs109392728 | 43831664 | 2.404 | −6.638 ± 2.302 | 0.143 | 0.089 | CHAT |
a BTC Bos Taurus chromosome
bIntervals containing individually validated SNPs are in bold
c MAF minor allele frequency
d σ 2d = dominance variance; σ 2p = phenotypic variance
eGenes with both top SNPs in discovery and validation inside them are in bold
fGenes with individually validated SNPs within them