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 |
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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) |
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last database update 07/05/2024 MGI 6.24 |
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