Skip to main content

Table 2 Distribution of ataxia phenotypes by the KCNJ10:g.22141027insC genotypes for Parson Russell (PRT) und Jack Russell Terriers (JRT)

From: Genome-wide association study for hereditary ataxia in the Parson Russell Terrier and DNA-testing for ataxia-associated mutations in the Parson and Jack Russell Terrier

Breed

Phenotype

 

KCNJ10:g.22141027insC

 

n

wt/wt

wt/mut

mut/mut

PRT

A

12

0

2

10

B

4

1

0

3

C

2

1

0

1

D

20

7

12

1

E

3

1

2

0

F

36

24

10

2

Subtotal

 

77

34

26

17

JRT

A

0

0

0

0

B

3

1

0

2

C

0

0

0

0

D

0

0

0

0

E

0

0

0

0

F

6

0

6

0

Subtotal

 

9

1

6

12

  1. A: hereditary ataxia clinically and histopathologically diagnosed, B: clinical signs of ataxia, C: clinical signs of ataxia according to the medical records of the veterinary clinic and report of the owner, D: unaffected dogs, E: unaffected dogs, but affected dogs in progeny or siblings, F: no information on health status; the phenotype group A contains 4 PRT shown in the pedigree (Pedigree numbers (P.n.) 14, 15, 16, 17, see Additional file 12), group D contains 7 PRT (P.n. 2, 6, 7, 8, 9, 10, 11, see Additional file 12) and group F includes 6 PRT (P.n. 1, 3, 4, 5, 12, 13, see Additional file 12)