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spinocerebellar ataxia type 27A (DOID:0050976)
Alliance: disease page
Synonyms: autosomal dominant congenital nystagmus 4; congenital nystagmus 4; SCA27A; spinocerebellar ataxia type 27; vestibulocerebellar disorder with predominant ocular signs
Alt IDs: OMIM:193003
Definition: An autosomal dominant cerebellar ataxia that is characterized by general cerebellar dysfunction manifest as gait disturbances, ataxia, tremor, dysarthria, and gaze-evoked nystagmus and has_material_basis_in heterozygous mutation in the FGF14 gene on chromosome 13q33. Some patients have heterozygous deletions of chromosome 13q33 affecting the FGF14 and ITGBL1 genes, which may thus be considered a contiguous gene deletion syndrome.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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03/25/2025
MGI 6.24 		The Jackson Laboratory