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Human Disease and Mouse Model Detail
Human Disease Episodic Ataxia, Type 2; EA2
OMIM ID: 108500
Synonyms Acetazolamide-Responsive Hereditary Paroxysmal Cerebellar Ataxia; APCA; Ataxia, Episodic, with Nystagmus; Ataxia, Familial Paroxysmal; Cerebellar Ataxia, Paroxysmal, Acetazolamide-Responsive; CAPA; Cerebellopathy, Hereditary Paroxysmal; Episodic Ataxia; Episodic Ataxia, Nystagmus-Associated
View all models View ALL (1) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     CACNA1A* Cacna1a* View 1 model HomoloGene and HGNC
References Disease References using Mouse Models (1)

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 6.0
The Jackson Laboratory