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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; Night Blindness, Congenital Stationary, Type 2; CSNB2
View all models View ALL (7) 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 7 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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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory