|
Symbol Name ID |
Kcnv2
potassium channel, subfamily V, member 2 MGI:2670981 |
| Darker colors indicate more annotations |
| Human Phenotypes | Astigmatism |
Macular atrophy |
Cone/cone-rod dystrophy |
Strabismus |
Horizontal nystagmus |
Myopia |
Nyctalopia |
Photophobia |
Reduced visual acuity |
Scotoma |
| Disease(s) Associated with KCNV2 | ||||||||||
| retinal cone dystrophy 3B |
| Mouse Phenotypes | increased retina apoptosis |
decreased retina rod cell number |
short photoreceptor inner segment |
short photoreceptor outer segment |
thin retina outer nuclear layer |
decreased total retina thickness |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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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 04/09/2024 MGI 6.23 |
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