Turnaround time
10 workdays
48.4
40
DNA test for the SLC37A2 variant c.1332C>T causing craniomandibular osteopathy / CMO in Cairn Terrier, Scottish Terrier and West Highland White Terrier.
Overview
This genetic test analyses the SLC37A2 variant c.1332C>T in Cairn Terrier, Scottish Terrier and West Highland White Terrier. The condition is known as craniomandibular osteopathy, CMO, Lion Jaw, Scotty Jaw and Westie Jaw.
CMO is a developmental disorder of the skull and jaw bones in young dogs. It is also known as craniomandibular osteopathy, CMO, Lion Jaw, Scotty Jaw and Westie Jaw. Signs often start around four to eight months of age and may include jaw swelling, pain, difficulty eating or opening the mouth, reduced appetite and periodic fever.
The trait is described as autosomal dominant with incomplete penetrance. C/C means the tested variant was not detected. C/T means one copy of the variant is present and the dog carries genetic risk for CMO. T/T means two copies are present; severity may vary because penetrance is incomplete, but this is a genetically high-risk result.
Included subanalyses
This analysis includes the following subanalysis:
Allele combinations & result interpretations
Below, for each tested locus, you will find the possible allele combinations that may be reported within this analysis, together with a brief explanation of their genetic meaning. The interpretation of possible interactions between different loci is included in the report, but is not shown here in full because that would lead to too many combinations on this page. The final expression may also depend on other genes and their interaction.
Genotype / allele combination: Clear / normal genotype (C/C)
The genotype C/C means the tested SLC37A2 variant was not detected. This dog does not pass this variant to offspring.
Genotype / allele combination: Carrier / variant carrier (C/T)
The genotype C/T means one copy of the tested SLC37A2 variant is present. Because inheritance is autosomal dominant with incomplete penetrance, this increases CMO risk and the variant can be passed to about half of offspring.
Genotype / allele combination: Affected or high-risk genotype (T/T)
The genotype T/T means two copies of the tested SLC37A2 variant are present. This is a genetically high-risk result for CMO; visible severity can differ because penetrance is incomplete, but it should be treated as an important breeding risk profile.
Sampling and submission guidelines





References