Affected gene: KCNJ10  
Inheritance: Autosomal recessive  
Mutation: CanFam3.1 38 g.22140659T>C c.986T>C  
OMIA link: 002089-9615  

Breeds appropriate for testing: Belgian Shepherd Malinois, Belgian Shepherd Groenedael, Belgian Shepherd Laekenois,Belgian Shepherd Tervueren.

References:  
Mauri, N., Kleiter, M., Leschnik, M., Högler, S., Dietschi, E., Wiedmer, M., Dietrich, J., Henke, D., Steffen, F., Schuller, S., Gurtner, C., Stokar-Regenscheit, N., O'Toole, D., Bilzer, T., Herden, C., Oevermann, A., Jagannathan, V., Leeb, T. (2017). A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1). G3 (Bethesda) 7:663-669. PubMed reference: 28007838. DOI: 10.1534/g3.116.038455.