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Human Disease and Mouse Model Detail
Human Disease Night Blindness, Congenital Stationary, Type 2A; CSNB2A
OMIM ID: 300071
Synonyms Csnb, Incomplete, X-Linked; Night Blindness, Congenital Stationary, Type 2; CSNB2
View all models View ALL (4) mouse models for this human disease.
Genes and
mouse models 		Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Cacna1f* CACNA1F* View 4 models 1:1 Homology
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
05/22/2013
MGI 5.13 		The Jackson Laboratory