Affected Gene: MYBPC3
Transmission: Autosomal dominant
Mutation: Felis_catus_9.0 D1 g.101340772C>G c.91G>C
OMIA Link: 000515-9685

Breeds Recommended for Testing: Maine Coon

References:
Meurs, K.M., Sanchez, X., David, R.M., Bowles, N.E., Towbin, J.A., Reiser, P.J., Kittleson, J.A., Munro, M.J., Dryburgh, K., Macdonald, K.A., Kittleson, M.D.
A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.
Hum Mol Genet 14:3587-93, 2005. PubMed: 16236761
DOI: 10.1093/hmg/ddi386
O'Donnell, K., Adin, D., Atkins, C.E., DeFrancesco, T., Keene, B.W., Tou, S., Meurs, K.M.
Absence of known feline MYH7 and MYBPC3 variants in a diverse cohort of cats with hypertrophic cardiomyopathy.
Anim Genet 52:542-4, 2021. PubMed: 33970514
DOI: 10.1111/age.13074