Table 1.
Genome scan1 | SSC2 | Pos3 | Marker4 | Min/Maj5 | MAF6 | β 7 | P 8 | QTLs9 | Genes10 |
---|---|---|---|---|---|---|---|---|---|
Italian Large White | |||||||||
Haplotype‐based | 7 | 97435001 | CHR7_B973 | H/N | 0.426 | 0.188 | 1.61 × 10−15 | NNF, TVN, VN | ENTPD5, FAM161B, VRTN, ABCD4, ALDH6A1, SYNDIG1L, VSX2, BBOF1, COQ6, LIN52, ZNF410 |
Single‐marker | 7 | 97652632 | MARC0038565 | A/G | 0.482 | −0.163 | 2.65 × 10−12 | TVN | VRTN , SYNDI1GL |
Single‐marker | 10 | 47751164 | M1GA0014145 | A/G | 0.477 | −0.135 | 2.83 × 10−8 | – | FRMD4A |
Haplotype‐based | 10 | 48035001 | CHR10_B479 | H/N | 0.367 | −0.129 | 1.56 × 10−8 | LTN | FRMD4A , PRPF18, BEND7 |
Single‐marker | 12 | 24723142 | MARC0031045 | G/A | 0.358 | 0.117 | 1.03 × 10−6 | THVN | SKAP1, HOXB1 |
Italian Landrace | |||||||||
Haplotype‐based | 3 | 120600001 | CHR3_B1205 | H/N | 0.014 | −1.048 | 8.40 × 10−8 | THVN | RAD51AP2, FAM49A |
Haplotype‐based | 6 | 113000001 | CHR6_B1129 | H/N | 0.062 | −0.466 | 1.95 × 10−7 | – | CDH2 |
Haplotype‐based | 8 | 4500001 | CHR8_B44 | H/N | 0.011 | −1.142 | 9.30 × 10−9 | NFN | C8H4orf50, JAKMIP1, WFS1, LOC102165510, PPP2R2C |
Haplotype‐based | 11 | 18900001 | CHR11_B188 | H/N | 0.034 | −0.529 | 1.55 × 10−7 | – | FNDC3A, CYSLTR2, RCBTB2 |
Haplotype‐based | 13 | 189100001 | CHR13_B1890 | H/N | 0.016 | −0.957 | 5.43 × 10−9 | MI | ATP5J, GABPA, JAM2, MRPL39 |
Haplotype‐based | 14 | 132300001 | CHR14_B1322 | H/N | 0.014 | −0.953 | 1.73 × 10−7 | – | C14H10orf120, LOC100620521, AWN, LOC100519221, FAM24B, SPMI, DMBT1, PSP‐II, AQN‐1, HTRA1, PSP‐I |
Haplotype‐based | 14 | 114800001 | CHR14_B1147 | H/N | 0.051 | −0.547 | 1.79 × 10−7 | – | COL17A1, SH3PXD2A, STN1, SLK |
Single‐marker | 14 | 23582019 | WU_10.2_14_25047530 | A/G | 0.078 | −0.445 | 3.18 × 10−7 | – | SFSWAP |
Haplotype‐based | 15 | 134400001 | CHR15_B1343 | H/N | 0.030 | −0.951 | 8.08 × 10−16 | BW, BL, LW, TNBA, LS |
TRPM8, SPP2 Close to ARL4C |
Haplotype‐based | 15 | 19300001 | CHR15_B192 | H/N | 0.013 | −0.877 | 6.29 × 10−8 | – | NCKAP5 |
Haplotype‐based | 16 | 57400001 | CHR16_B573 | H/N | 0.024 | −0.806 | 6.15 × 10−8 | – | TENM2 |
Haplotype‐based | 16 | 68700001 | CHR16_B686 | H/N | 0.017 | −0.993 | 5.08 × 10−9 | – | SAP30L, HAND1, GALNT10 |
Genome scans performed within each pig population. SNPs and Haplotypes indicate which DNA markers have been used to carry out the genome scans.
Sus scrofa chromosome.
Position, in bp, on the Sus scrofa reference genome (v.11.1).
DNA marker identifier reported in the chip panels. For haplotypes, the haploblock identifier (chromosome specific) is reported.
Minor/Major alleles. Haplotypes have been treated as bi‐allelic variants (H = haplotype allele and N = other N alleles).
Minor allele frequency.
Regression coefficient. A positive value indicates that the no. of teats increases with the increasing of the number of copies of the minor allele. A negative value indicates that the no. of teats decreases with the increasing of the number of copies of the minor allele.
P at the Wald test (GEMMA).
QTLs related to reproductive traits overlapping the association peaks. Short names for QTL are: BL, body length; BW, body width; LS, litter size; LTN, left teat number; LWT, litter weight; MI, maternal infanticide; NFN, non‐functional nipples; NNF, number of non‐viable foetuses; THVN, thoracolumbar vertebra number; TNBA, total number of born alive; TVN, thoracic vertebra number; VN, vertebra number.
Genes overlapping the haplotype or closed to a SNP. The candidate genes are reported in bold.