About   Help   FAQ
Support MGI: answer a 5-question survey
Human Disease and Mouse Model Detail
Human Disease Night Blindness, Congenital Stationary, Type 1D; CSNB1D
OMIM ID: 613830
Synonyms Csnb, Complete, Autosomal Recessive; Night Blindness, Congenital Stationary
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...
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Slc24a1 SLC24A1*   1:1 Homology
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
01/20/2015
MGI 5.21 		The Jackson Laboratory