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Symbol Name ID |
Ift140
intraflagellar transport 140 MGI:2146906 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Cataract |
Posterior subcapsular cataract |
Optic atrophy |
Optic disc pallor |
Macular degeneration |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Retinal dystrophy |
Rod-cone dystrophy |
Hypertelorism |
Abnormal electroretinogram |
Undetectable electroretinogram |
Nystagmus |
Ophthalmoplegia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Blindness |
Peripheral visual field loss |
Visual loss |
Glaucoma |
| Disease(s) Associated with IFT140 | |||||||||||||||||||||||||||
| retinitis pigmentosa | |||||||||||||||||||||||||||
| short-rib thoracic dysplasia 9 with or without polydactyly |
| Mouse Phenotypes | anophthalmia |
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| Availability | Mouse Genotype | |
| Ift140cauli/Ift140cauli | ||
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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