|
Symbol Name ID |
Cnga1
cyclic nucleotide gated channel alpha 1 MGI:88436 |
| 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 |
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 |
Reduced visual acuity |
Blindness |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with CNGA1 | ||||||||||||||||||||||
| retinitis pigmentosa | ||||||||||||||||||||||
| retinitis pigmentosa 49 |
| Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
photoreceptor inner segment degeneration |
photoreceptor outer segment degeneration |
retina cone cell degeneration |
retina rod cell degeneration |
abnormal ocular fundus morphology |
abnormal retina inner nuclear layer morphology |
retina outer nuclear layer degeneration |
retina degeneration |
abnormal electroretinogram waveform feature |
decreased a-wave amplitude |
decreased b-wave amplitude |
blindness |
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| Availability | Mouse Genotype | ||||||||||||||
| Cnga1m1Mhda/Cnga1m1Mhda | |||||||||||||||
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 04/30/2024 MGI 6.23 |
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