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. 2018 Aug 6;50:40. doi: 10.1186/s12711-018-0412-z

Table 4.

Individual and overlapping QTL regions for semen traits in L2

Chra QTL region (Mb)b Nb SNPc Var (%)d Var (%) Var (%) Var (%) Candidate geneg
MOTe PROMOT lnNcells ABN
1 270.94–271.74 10 -f 9.1 -h
1 55.61–56.47 26 2.4 1.4
2 145.69–146.49 16 5.2 NME5
2 154.03–154.83 23 4.3
3 110.29–111.09 19 3.6
6 83.32–84.12 12 4.7 AZIN2
7 116.37–117.28 25 1.4 3.3 SPATA7
7 82.56–83.36 10 1.0 2.4 METTL3
8 133.90–134.94 20 5.9 10.8 HPGDS
9 36.46–37.26 12 8.0
9 9.32–10.31 19 1.0 1.7
11 41.05–41.85 11 3.5 1.6
13 11.35–12.15 19 4.3
13 107.48–108.28 10 8.0
15 37.17–37.97 20 4.9
18 42.80–43.60 19 4.0

aChromosome

bPosition of QTL region

cNumber of SNPs within the QTL region

dPercentage of genetic variance explained by the QTL region

eSemen traits: MOT: sperm motility; PROMOT: sperm progressive motility; lnNcells: number of sperm cells per ejaculate; ABN: total morphological abnormalities

fThe percentage of genetic variance explained by the QTL region is < 1%. When the variance is reported for more than one trait, the QTL region is overlapping across traits

gBest candidate gene(s) in the region

hNo candidate genes associated with the trait