About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Night Blindness, Congenital Stationary, Type 1A; CSNB1A
OMIM ID: 310500
Synonyms Csnb, Complete, X-Linked; Hemeralopia-Myopia; Night Blindness, Congenital Stationary; Night Blindness, Congenital Stationary, with Myopia
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

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Nyx* NYX* View 1 model 1:1 Homology
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
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
10/08/2014
MGI 5.20
The Jackson Laboratory