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Symbol Name ID |
Iqcb1
IQ calmodulin-binding motif containing 1 MGI:2443764 |
| Darker colors indicate more annotations |
| Human Phenotypes | Keratoconus |
Cataract |
Abnormal optic disc morphology |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Retinal dystrophy |
Rod-cone dystrophy |
Perifoveal hypoautofluorescence |
Abnormal electroretinogram |
Undetectable electroretinogram |
Nystagmus |
Rotary nystagmus |
High myopia |
Color vision defect |
Nyctalopia |
Photophobia |
Visual impairment |
Reduced visual acuity |
Amblyopia |
Congenital blindness |
Severely reduced visual acuity |
Constriction of peripheral visual field |
Ring scotoma |
Visual loss |
Progressive visual loss |
| Disease(s) Associated with IQCB1 | ||||||||||||||||||||||||||
| Leber congenital amaurosis | ||||||||||||||||||||||||||
| nephronophthisis | ||||||||||||||||||||||||||
| retinitis pigmentosa 3 | ||||||||||||||||||||||||||
| Senior-Loken syndrome |
| Mouse Phenotypes | increased cornea thickness |
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| Availability | Mouse Genotype | |
| Iqcb1em1(IMPC)Bay/Iqcb1+ | ||
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 04/09/2024 MGI 6.23 |
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