|
Symbol Name ID |
Prpf8
pre-mRNA processing factor 8 MGI:2179381 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Cystoid macular edema |
Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Subcapsular cataract |
Posterior subcapsular cataract |
Optic atrophy |
Optic disc drusen |
Optic disc pallor |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Rod-cone dystrophy |
Perifoveal ring of hyperautofluorescence |
Asteroid hyalosis |
Abnormal electroretinogram |
Nystagmus |
Ophthalmoplegia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Blindness |
Constriction of peripheral visual field |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with PRPF8 | |||||||||||||||||||||||||||
| retinitis pigmentosa | |||||||||||||||||||||||||||
| retinitis pigmentosa 13 |
| Mouse Phenotypes | vision/eye phenotype |
abnormal retina pigment epithelium morphology |
retina degeneration |
|
| Availability | Mouse Genotype | |||
| Prpf8tm1.1Eap/Prpf8tm1.1Eap | * | |||
| Prpf8tm1.1Eap/Prpf8+ | * | |||
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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