Table 1.
Traita | Startb (bp) | Endc (bp) | No. significant SNPsd | Most significant SNP | |||
---|---|---|---|---|---|---|---|
| |||||||
−log10Pe | Positionf (bp) | σ2pg (%) | Geneh | ||||
Carcass weight | |||||||
1 | 33,542,443 | 33,785,060 | 4 | 4.06 | 33,705,065 | 16.4 | GRID2 |
2 | 36,886,556 | 36,911,817 | 1 | 3.03 | 36,899,187 | 6.4 | HERC3 |
3 | 40,720,193 | 41,056,099 | 5 | 3.51 | 40,759,899 | 6.1 | SLIT2 |
4 | 44,327,199 | 44,337,254 | 2 | 3.34 | 44,288,037 | 8.1 | LOC782350 |
5 | 54,156,738 | 54,328,469 | 1 | 3.20 | 54,242,604 | 9.3 | LOC100138865 |
Backfat thickness | |||||||
1 | 17,173,803 | 17,810,293 | 2 | 3.21 | 17,773,728 | 7.6 | COL25A1 |
2 | 33,689,670 | 33,989,255 | 6 | 4.03 | 33,897,434 | 5.1 | GRID2 |
3 | 54,526,954 | 54,918,598 | 3 | 3.31 | 54,808,804 | 5.0 | LOC100138865 |
Longissimus dorsi muscle area | |||||||
1 | 33,521,996 | 33,620,177 | 3 | 3.76 | 33,569,479 | 10.5 | GRID2 |
2 | 39,531,541 | 39,604,431 | 1 | 4.30 | 39,567,986 | 10.9 | LOC100138489 |
3 | 51,811,957 | 54,085,642 | 5 | 4.04 | 52,006,701 | 9.0 | LOC784827 |
4 | 110,285,672 | 110,633,096 | 11 | 4.99 | 110,360,573 | 8.5 | ZNF518B |
5 | 113,430,135 | 113,492,277 | 1 | 3.02 | 113,461,206 | 4.3 | BOD1L |
Marbling score | |||||||
1 | 76,580,801 | 76,626,038 | 1 | 3.11 | 76,603,420 | 5.7 | LOC100138549 |
2 | 108,330,907 | 108,370,731 | 1 | 3.24 | 108,350,819 | 7.2 | STK32B |
Number of QTL region for each trait.
The positions of the SNP markers and genes were based on the bovine reference genome (btau4.0).
The positions of the boundary SNPs flanking the QTL region.
Number of significant SNPs that were detected within the QTL region.
Negative logarithm of the comparison-wise p value of the test-statistic for the SNP with the most strong signal (statistical evidence) against the null hypothesis of no QTL at the SNP position.
The SNP position with the most strong signal.
The fraction of the trait phenotypic variance due to the SNP, computed as , in which σh2, σs2, and σe2 are variance estimates due to SNP (haplotype), sires, and residuals in the LDVCM analysis (Blott et al., 2003).
The gene that was closest to the most significant SNP.