Symbol Name ID |
Kcnj13
potassium inwardly-rectifying channel, subfamily J, member 13 MGI:3781032 |
Darker colors indicate more annotations |
Human Phenotypes | Photophobia |
Disease(s) Associated with KCNJ13 | |
Leber congenital amaurosis 16 |
Mouse Phenotypes | absent suckling reflex |
|
Availability | Mouse Genotype | |
Kcnj13tm1(KOMP)Vlcg/Kcnj13tm1(KOMP)Vlcg |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|