Table 2. Closest SNP, confidence interval, and protein-coding gene content of semilandmark QTL.
QTL | Closest SNP | Chr | Left | Pos | Right | Replic. | nPCGa | nCG.2Db | nCG.3D | CG.Semic |
---|---|---|---|---|---|---|---|---|---|---|
SH1 | gnf01.075.385 | 1 | 42.33 | 43.62 | 44.33 | 2D, 3D | 56 | 4 | ||
SH2 | rs3722345 | 2 | 51.09 | 51.09 | 60.54 | 2D, 3D | 243 | 2 | 2 | |
SH3 | rs6274061 | 3 | 12.01 | 20.01 | 21.01 | 81 | 2 | |||
SH4 | rs3676039 | 3 | 59.01 | 65.01 | 77.01 | 115 | 2 | Lef1 | ||
SH5 | rs3711477 | 4 | 52.01 | 52.20 | 53.01 | 3D | 12 | 1 | ||
SH6 | UT_4_132.137715 | 4 | 81.01 | 83.01 | 84.01 | 44 | Rere | |||
SH7 | rs13478154 | 5 | 13.50 | 15.71 | 17.50 | 2D, 3D | 75 | 6 | 9 | Shh, Drc1, Ift172 |
SH8 | rs13478388 | 5 | 43.50 | 52.50 | 56.50 | 2D, 3D | 345 | 12 | 6 | Ambn, Fras1, Prkg2, Dmp1, Idua, Fgfrl1, Mn1, Kctd10 |
SH9 | CEL-6_86289708 | 6 | 41.55 | 43.00 | 43.00 | 2D, 3D | 3 | 4 | 3 | |
SH10 | rs3658783 | 6 | 84.00 | 88.00 | 89.28 | |||||
SH11 | rs13479427 | 7 | 43.05 | 55.02 | 57.20 | 477 | Akap13, Kif7, Serpinh1, Folr1 | |||
SH12 | rs6386110 | 8 | 22.38 | 25.52 | 27.52 | 2D, 3D | 69 | 1 | 7 | |
SH13 | rs3721056 | 9 | 43.10 | 44.47 | 71.10 | 2D, 3D | 366 | 2 | 2 | Atr, Ryk |
SH14 | rs3686911 | 10 | 3.03 | 3.18 | 9.03 | 48 | ||||
SH15 | mCV24217147 | 10 | 67.03 | 70.03 | 71.12 | 2D, 3D | 24 | 3 | 1 | |
SH16 | rs3700830 | 11 | 12.08 | 16.08 | 17.08 | 52 | ||||
SH17 | rs13481127 | 11 | 48.08 | 49.08 | 54.08 | 2D, 3D | 116 | |||
SH18 | rs3672597 | 11 | 82.08 | 84.08 | 86.08 | 2D, 3D | 106 | |||
SH19 | rs13481321 | 12 | 6.90 | 7.99 | 8.95 | 3D | 44 | |||
SH20 | rs3693942 | 13 | 25.00 | 26.00 | 26.52 | 2D, 3D | 36 | |||
SH21 | CEL-15_36490596 | 15 | 13.68 | 13.68 | 14.99 | 2D, 3D | 32 | |||
SH22 | rs4204106 | 16 | 33.03 | 48.03 | 53.31 | 2D, 3D | 177 | |||
SH23 | rs6298471 | 17 | 16.03 | 18.14 | 21.14 | 314 |
QTL, quantitative trait loci; Chr, chromosome; Pos, position; Replic, replication, nPCG, number of protein coding genes; nCG, number of candidate genes; SH, shape etc.
Number of protein-coding genes in the interval.
Number of candidate genes annotated for “mandible” in the MGI databases in the QTL confidence interval from 2D or 3D datasets.
Candidate genes annotated for “mandible” in the MGI databases in the QTL confidence interval for the semilandmark analysis. Candidates with nonsynonymous or splice-site variants between AJ and C57BL/6J are indicated in bold.