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Human Disease and Mouse Model Detail
Human Disease Night Blindness, Congenital Stationary, Type 1D; CSNB1D
OMIM ID: 613830
Human Phenotype Ontology associations
Synonyms Csnb, Complete, Autosomal Recessive; Night Blindness, Congenital Stationary
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     SLC24A1* Slc24a1* View 1 model HomoloGene and HGNC
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
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Send questions and comments to User Support. 		last database update
09/20/2016
MGI 6.05 		The Jackson Laboratory