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Symbol Name ID |
Arhgef18
Rho/Rac guanine nucleotide exchange factor 18 MGI:2142567 |
| 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 |
Abnormal electroretinogram |
Nystagmus |
Ophthalmoplegia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Blindness |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with ARHGEF18 | ||||||||||||||||||||
| retinitis pigmentosa |
| Mouse Phenotypes | abnormal retina morphology |
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| Availability | Mouse Genotype | |
| Arhgef18tm1b(KOMP)Mbp/Arhgef18+ | ||
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 04/16/2024 MGI 6.23 |
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