Australian Stumpy Tail Cattle Dog
Bouvier australien courte queue, Perro pastor australiano stumpy tail Australian töpöhäntäinen karjakoira
FCI Group
Sheepdogs and Cattledogs (except Swiss Cattledogs)
AKC Group
Foundation Stock Service
TKC Group
Not Recognized
Country of Origin
AU
Health Testing Requirements by Country
Skeletal and Muscular
FI
Test Relevances
Neuronal Ceroid Lipofuscinosis 5 (NCL5)
Some Relevance
Primary Lens Luxation (PLL)
Some Relevance
Progressive Retinal Atrophy (PRA-prcd)
Some Relevance
Tail length, Short
Some Relevance
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Cystinuria Type I-A
No Evidence
Degenerative Myelopathy
No Evidence
Myotonia Congenita
No Evidence
Von Willebrand Disease I
No Evidence
Neuronal Ceroid Lipofuscinosis 5 (NCL5)
Some Relevance
Primary Lens Luxation (PLL)
Some Relevance
Findings indicate the mutation segregates in a large number of different breeds of dog, many of which are terriers or breeds with terrier co?ancestry, but some of which have more diverse origins. Research indicates that the mutation is present at high frequency within most of the breeds in which it segregates. (Gould et. al, 2011)
Progressive Retinal Atrophy (PRA-prcd)
Some Relevance
Tail length, Short
Some Relevance
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Cystinuria Type I-A
No Evidence
Possibly incorrect mutation for this breed. See cystinuria type II-A
Degenerative Myelopathy
No Evidence
Both clinically rare and of complex inheritance. Test is considered poorly correlated with risk for development of DM, and recommendations are to not use the test for breed-wide breeding strategies. While the SOD 1 variant may be commonly found across many breeds, there are few clinical cases observed and confirmed, and in many cases DM has never been observed in the breeds.
Myotonia Congenita
No Evidence
Von Willebrand Disease I
No Evidence
Mutation is widespred, so may be relevant
- Updated