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Table 2 Chromosome-wise significant (p < 0.05) SNPs associated with footrot

From: Genome-wide association study of footrot in Texel sheep

Chr

SNP

Position (bp)

Model*

-log10 (p-value)

Variance explained ‡

Nearest gene

Function

Name

Distance † (bp)

4

s55696.1

66980883

R

4.77

0.054

CPVL

between exons 2 & 3

carboxypeptidase, vitellogenic-like protein

8

OAR8_77678255.1

72284055

A

4.59

0.052

HNRPDL

455966

heterogeneous nuclear ribonucleoprotein D-like

Uncharacterised (72529599–72531004)

−245544

unknown

14

s53098.1

8589373

R

4.50

0.051

Uncharacterised (8581480–8673246)

between exons 1 & 2

unknown

17

OAR17_29456634.1

26848221

R

4.52

0.051

Uncharacterised (26721069–26722410)

125811

unknown

18

OAR18_23478564.1

23886219

A

4.88

0.056

Uncharacterised (23697715–23776771)

109448

unknown

D

5.65

0.065

MORF4L1

−288749

mortality factor 4 like 1

24

s34109.1

962868

D

4.35

0.049

Uncharacterised (961975–993337)

between exons 8 & 7

unknown

26

OAR26_8299529.1

6166783

R

4.50

0.051

GPM6A

24644

glycoprotein M6A

Uncharacterised (6232840–6233142)

−66057

unknown

  1. † Positive value denotes the gene located downstream of SNP, negative value denotes the gene located upstream of SNP.
  2. ‡ proportion of variance explained by the SNP.
  3. * A – additive; R – recessive; D – dominant model.