Symbol Name ID |
Kcnv2
potassium channel, subfamily V, member 2 MGI:2670981 |
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 |
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Availability | Mouse Genotype | |||
Kcnv2tm1.2(KOMP)Wtsi/Kcnv2tm1.2(KOMP)Wtsi |
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 |
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