Table 1.
Location of the most significant QTL, limited to the top five per breed, which were associated with development of hind quarter and the genes located within these QTL within each breed
Breed | Chr | Start | End | Number of suggestive and significant SNPs | Most significant SNP | p-value | Allele frequency of + allele | Candidate genes within this QTL | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
AA | CH | HE | LM | SI | ||||||||
AA | 1 | 72069526 | 130071811 | 8 | 120584401a | 3.69 × 10−6 | 0.940 | 0.940 | 0.061 | 0.949 | 0.951 | DLG1, FAM43A, APOD, OPA1, OSTN, GHSR |
8 | 72017409 | 73103211 | 16 | 72569526b | 3.25 × 10−6 | 0.276 | 0.565 | 0.264 | 0.332 | 0.687 | ADAM28 | |
10 | 5155837 | 6179062 | 11 | 5655837d | 7.60 × 10−6 | 0.032 | 0.133 | 0.000 | 0.073 | 0.036 | SFXN1, DRD1e | |
23 | 20541063 | 21541072 | 2 | 21041063b | 3.34 × 10−7 | 0.995 | 0.977 | 0.000 | 0.000 | 0.005 | PTCHD4e | |
24 | 35913368 | 37107434 | 16 | 36567715a | 8.07 × 10−7 | 0.918 | 0.050 | 0.958 | 0.941 | 0.903 | ENOSF1, ADCYAP1 | |
CH | 2 | 35194 | 10711228 | 5128 | 6808074a | 9.07 × 10−49 | 0.000 | 0.079 | 0.000 | 0.028 | 0.004 | WDR75f, ASNSD1f, ARHGEF4f, MYO7Bf, IWS1e, NAB1f, MFSD6f, MSTNf, PMS1f, ORMDL1e, COL3A1f, COL5A2f, ANKARf, SLC40A1f |
4 | 89299122 | 90487119 | 12 | 89799122a | 4.67 × 10−6 | 0.000 | 0.007 | 0.002 | 0.000 | 0.992 | GPR37e, POT1 | |
14 | 33353270 | 34360874 | 4 | 33855595a | 2.20 × 10−7 | 0.013 | 0.026 | 0.054 | 0.054 | 0.982 | PREX2 | |
21 | 34538609 | 35572213 | 47 | 35062974b | 9.70 × 10−7 | 0.617 | 0.521 | 0.594 | 0.000 | 0.451 | UBL7, SEMA7A, PML | |
28 | 15669176 | 18516719 | 77 | 16273851a | 2.95 × 10−8 | 0.574 | 0.827 | 0.580 | 0.416 | 0.520 | ANK3, CDK1, RHOBTB1 | |
HE | 1 | 68813144 | 73614763 | 228 | 69348458b | 5.23 × 10−7 | 0.764 | 0.531 | 0.237 | 0.317 | 0.480 | KALRNe, ITGB5e |
7 | 83591608 | 84673367 | 26 | 84122153a | 3.16 × 10−7 | 0.177 | 0.851 | 0.913 | 0.000 | 0.910 | ACOT12, ATG10 | |
12 | 48965278 | 50129513 | 4 | 49465278a | 1.84 × 10−6 | 0.020 | 0.995 | 0.996 | 0.983 | 0.000 | KLF12 | |
13 | 2761800 | 3761897 | 2 | 3261897a | 7.44 × 10−7 | 0.681 | 0.761 | 0.795 | 0.269 | 0.695 | MRPL33 | |
23 | 12056019 | 13111217 | 5 | 12571991b | 1.09 × 10−6 | 0.220 | 0.000 | 0.094 | 0.885 | 0.100 | GLO1, GLP1R | |
LM | 2 | 4293223 | 12640428 | 2610 | 6622189a | 3.22 × 10−30 | 0.491 | 0.447 | 0.250 | 0.043 | 0.799 | WDR75, ASNSD1f, MYO7B, IWS1, NAB1f, MFSD6e, MSTNf, PMS1f, ORMDL1e, COL3A1f, COL5A2f, ANKARf, SLC40A1f, ZNF804A |
2 | 13916060 | 14987913 | 113 | 14446207bc | 4.83 × 10−8 | 0.567 | 0.562 | 0.374 | 0.394 | 0.523 | PDE1Ae, PPP1R1C | |
5 | 59612855 | 60696179 | 7 | 60112855a | 1.58 × 10−7 | 0.000 | 0.000 | 0.000 | 0.997 | 0.996 | AMDHD1 | |
11 | 12163298 | 13181229 | 7 | 12676690a | 1.56 × 10−6 | 0.486 | 0.283 | 0.000 | 0.231 | 0.163 | CYP26B1, DYSF, ZNF638 | |
SI | 6 | 76112104 | 77238886 | 16 | 76612104a | 1.28 × 10−6 | 0.997 | 0.993 | 0.000 | 0.000 | 0.993 | ENSBTAG00000043492 |
7 | 103195804 | 104247192 | 3 | 103695804b | 1.78 × 10−6 | 0.000 | 0.000 | 0.000 | 0.005 | 0.005 | SLCO4C1e, SLC06A1 | |
9 | 65068999 | 66303927 | 4 | 65712927a | 4.56 × 10−7 | 0.000 | 0.000 | 0.000 | 0.003 | 0.996 | TBX18e, MRAP2 | |
23 | 41204249 | 42287354 | 9 | 41747427a | 1.48 × 10−7 | 0.009 | 0.008 | 0.994 | 0.962 | 0.990 | JARID2 | |
25 | 22649471 | 23937019 | 6 | 23400365a | 1.00 × 10−7 | 0.985 | 0.993 | 0.000 | 0.993 | 0.998 | AQP8, ZKSCAN2 |
SNP classification: aintergenic, bintron, cupstream gene variant ddownstream gene variant
Significance of SNPs within genes: egene contained at least one suggestive SNP, fgene contained at least one significant SNP