Symbol Name ID |
Gnat1
G protein subunit alpha transducin 1 MGI:95778 |
Darker colors indicate more annotations |
Human Phenotypes | Optic disc pallor |
Congenital stationary night blindness |
Rod-cone dystrophy |
Visual impairment |
Constriction of peripheral visual field |
Disease(s) Associated with GNAT1 | |||||
congenital stationary night blindness 1G | |||||
congenital stationary night blindness autosomal dominant 3 |
Mouse Phenotypes | short retina rod cell outer segment |
abnormal retina neuronal layer morphology |
thin retina inner nuclear layer |
thin retina outer nuclear layer |
increased susceptibility to age-related retinal degeneration |
abnormal eye physiology |
abnormal eye electrophysiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
|
Availability | Mouse Genotype | |||||||||
Gnat1irdr/Gnat1irdr | ||||||||||
Gnat1tm1Clma/Gnat1tm1Clma |
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 04/16/2024 MGI 6.23 |
|
|