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Human Disease and Mouse Model Detail
Human Disease Spinocerebellar Ataxia 15; SCA15
OMIM ID: 606658
Human Phenotype Ontology associations
Synonyms Spinocerebellar Ataxia; Spinocerebellar Ataxia 16, Formerly; SCA16, FORMERLY
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory