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

Table 3.

Individual and overlapping QTL regions for semen traits in L1

Chra QTL region (Mb)b Nb SNPc Var (%)d Var (%) Var (%) Var (%) Candidate geneg
MOTe PROMOT lnNcells ABN
1 135.51–136.31 17 1.2 1.2 -f 6.0 -h
1 255.48–256.28 17 1.2 1.5
1 290.90–291.84 25 1.0 1.3
1 305.18–305.98 23 4.6
3 28.53–29.33 18 1.0 2.9
4 28.25–29.05 12 2.5 6.4 5.9
4 84.90–85.73 21 1.4 2.5
4 123.12–124.20 30 1.8 1.0 1.3
5 17.61–18.47 26 7.5 3.0 SCN8A
6 8.24–9.13 20 2.6 1.1
8 16.06–16.86 20 3.2 1.7
9 139.53–140.63 23 1.8 4.3 5.6 PTGS2, PLA2G4A
10 10.58–11.45 23 1.2 1.5 1.0 6.9
12 6.23–7.03 32 3.4 DNAI2
12 40.76–41.56 17 1.2 1.7
13 143.61–144.69 13 1.2 1.0 IQCG
14 4.13–5.22 19 1.5 8.7 3.7 LOC102167830
14 72.83–73.63 16 6.8
14 99.70–100.51 25 1.7 1.2
15 61.93–62.73 15 3.5

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