Symbol Name ID |
Rp2
retinitis pigmentosa 2 homolog MGI:1277953 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Cataract |
Posterior subcapsular cataract |
Chorioretinal degeneration |
Optic atrophy |
Optic disc pallor |
Bull's eye maculopathy |
Abnormality of retinal pigmentation |
Pigmentary retinopathy |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Rod-cone dystrophy |
Fundus atrophy |
Abnormal electroretinogram |
Nystagmus |
Ophthalmoplegia |
Myopia |
High myopia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Blindness |
Constriction of peripheral visual field |
Peripheral visual field loss |
Central scotoma |
Pericentral scotoma |
Ring scotoma |
Glaucoma |
Disease(s) Associated with RP2 | ||||||||||||||||||||||||||||||||
retinitis pigmentosa | ||||||||||||||||||||||||||||||||
retinitis pigmentosa 2 |
Mouse Phenotypes | vision/eye phenotype |
decreased retina cone cell number |
abnormal retina photoreceptor morphology |
disorganized photoreceptor outer segment |
thin retina outer nuclear layer |
increased susceptibility to age-related retinal degeneration |
abnormal eye physiology |
abnormal electroretinogram waveform feature |
decreased a-wave amplitude |
abnormal b-wave amplitude |
decreased b-wave amplitude |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
abnormal vision |
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Availability | Mouse Genotype | ||||||||||||||
Rp2Gt(EUCJ0183f04)Hmgu/Rp2Gt(EUCJ0183f04)Hmgu | |||||||||||||||
Rp2tm1.1Asw/Rp2tm1.1Asw | * | ||||||||||||||
Rp2tm1.2Asw/Rp2tm1.2Asw | * | ||||||||||||||
Rp2Gt(EUCJ0183f04)Hmgu/Y | |||||||||||||||
Rp2tm1.2Asw/Y | * |
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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