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Symbol
Name
ID
Kcnv2
potassium channel, subfamily V, member 2
MGI:2670981
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Photophobia
Disease(s) Associated with KCNV2
retinal cone dystrophy 3B

Mouse Phenotypes
decreased retina rod cell number
short photoreceptor inner segment
short photoreceptor outer segment
Availability Mouse Genotype
Kcnv2tm1.2(KOMP)Wtsi/Kcnv2tm1.2(KOMP)Wtsi

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory