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Symbol Name ID |
Rp1l1
retinitis pigmentosa 1 homolog like 1 MGI:2384303 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cystoid macular edema |
Attenuation of retinal blood vessels |
Optic disc pallor |
Macular degeneration |
Macular dystrophy |
Bone spicule pigmentation of the retina |
Abnormal fundus fluorescein angiography |
Abnormal full-field electroretinogram |
Abnormal multifocal electroretinogram |
Exotropia |
Nyctalopia |
Reduced visual acuity |
Slow decrease in visual acuity |
| Disease(s) Associated with RP1L1 | |||||||||||||
| occult macular dystrophy | |||||||||||||
| retinitis pigmentosa 88 |
| Mouse Phenotypes | decreased retina photoreceptor cell number |
abnormal photoreceptor outer segment morphology |
short photoreceptor outer segment |
retina rod cell degeneration |
abnormal retina morphology |
thin retina outer nuclear layer |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | ||||||||
| Rp1l1tm1Jnz/Rp1l1tm1Jnz | |||||||||
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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