Collie Rough
Colley à poil long, Collie de pelo largo, Langhaariger Schottischer-Schäferhund, Rough Collie, Pitkäkarvainen skotlanninpaimenkoira, Pitkäkarvainen collie
FCI Group
Sheepdogs and Cattledogs (except Swiss Cattledogs)
AKC Group
Herding
TKC Group
Pastoral
Country of Origin
GB
Genetic Testing Breed-Specific Comment: Danish Rough Collie: Fredholm et al. (2016) reported that the deletion in NHEJ1 is not predictive for CH [choroidal hypoplasia] in the Danish Rough Collie population, despite appearing to be the same disease. It could be that the intronic deletion in NHEJ.
Health Testing Requirements by Country
Skin, Hair, and Nails
FI
Neurological and Neuromuscular
Skeletal and Muscular
UK
Ataxia, Locomotor, and Epilepsy
Eye Conditions and Blindness
Other Genetic Testing
Temperament
SE
Test Relevances
Multidrug Resistance 1 (MDR1)
Strong Relevance
Hyperuricosuria and Hyperuricemia (HUU)
Moderate Relevance
Canine Cyclic Neutropenia (Grey Collie Syndrome)
Some Relevance
Collie Eye Anomaly (CEA/CH)
Some Relevance
Degenerative Myelopathy
Some Relevance
Dermatomyositis
Some Relevance
Progressive Retinal Atrophy rcd2 (PRA-rcd2)
Some Relevance
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Hair, Long
No Evidence
Pyruvate Kinase Deficiency
No Evidence
Von Willebrand Disease I
No Evidence
Von Willebrand Disease II
No Evidence
Multidrug Resistance 1 (MDR1)
Strong Relevance
Hyperuricosuria and Hyperuricemia (HUU)
Moderate Relevance
Canine Cyclic Neutropenia (Grey Collie Syndrome)
Some Relevance
Collie Eye Anomaly (CEA/CH)
Some Relevance
May be relevant across many breeds, including those not specified in the literature, but of shared origins. Several reports have been raised that in some breeds the causality of the mutation may be complex. Clinical diagnosis may be especially important to the individual dog.
Degenerative Myelopathy
Some Relevance
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, even where there is some evidence of the presence of DM in the breed. 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.
Dermatomyositis
Some Relevance
Progressive Retinal Atrophy rcd2 (PRA-rcd2)
Some Relevance
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Hair, Long
No Evidence
Hair length testing has the potential relevance to any dog, but test usage is most often applied to those breeds with a heritage of these traits.
Pyruvate Kinase Deficiency
No Evidence
Von Willebrand Disease I
No Evidence
Mutation is widespred, so may be relevant
Von Willebrand Disease II
No Evidence
Connections
- Updated