|
Symbol Name ID |
Cngb1
cyclic nucleotide gated channel beta 1 MGI:2664102 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Posterior subcapsular cataract |
Optic atrophy |
Optic disc pallor |
Macular degeneration |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Rod-cone dystrophy |
Abnormal electroretinogram |
Nystagmus |
Ophthalmoplegia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Blindness |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with CNGB1 | ||||||||||||||||||||||
| retinitis pigmentosa | ||||||||||||||||||||||
| retinitis pigmentosa 45 |
| Mouse Phenotypes | vision/eye phenotype |
decreased retina photoreceptor cell number |
abnormal retina rod bipolar cell morphology |
abnormal retina horizontal cell morphology |
short retina rod cell outer segment |
abnormal retina rod cell outer segment morphology |
abnormal retina rod cell morphology |
retina photoreceptor degeneration |
abnormal retina pigment epithelium morphology |
thin retina outer nuclear layer |
decreased total retina thickness |
abnormal rod electrophysiology |
|
| Availability | Mouse Genotype | ||||||||||||
| Cngb1m1Btlr/Cngb1m1Btlr | |||||||||||||
| Cngb1tm1.1Biel/Cngb1tm1.1Biel | |||||||||||||
| Cngb1tm1.1Glf/Cngb1tm1.1Glf | * | ||||||||||||
| Cngb1tm1Sjpi/Cngb1tm1Sjpi | |||||||||||||
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 04/09/2024 MGI 6.23 |
|
|
|
||
Analysis Tools