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Human Disease and Mouse Model Detail
Human Disease Cone-Rod Synaptic Disorder, Congenital Nonprogressive; CRSD
OMIM ID: 610427
Synonyms Night Blindness, Congenital Stationary; Night Blindness, Congenital Stationary, Incomplete, Autosomal Recessive, Formerly; Night Blindness, Congenital Stationary, Type 2b, Formerly; CSNB2B, FORMERLY
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
     CABP4* Cabp4   HomoloGene and HGNC

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
MGI 6.01
The Jackson Laboratory