About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Episodic Ataxia, Type 2; EA2
OMIM ID: 108500
Human Phenotype Ontology associations
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 (2) 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 2 models HomoloGene and HGNC
References Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory