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Symbol
Name
ID
Rp2
retinitis pigmentosa 2 homolog
MGI:1277953
Phenotype annotations related to vision/eye
*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
Availability Mouse Genotype
Rp2Gt(EUCJ0183f04)Hmgu/Rp2Gt(EUCJ0183f04)Hmgu
Rp2tm1.1Asw/Rp2tm1.1Asw *
Rp2tm1.2Asw/Rp2tm1.2Asw *
Rp2Gt(EUCJ0183f04)Hmgu/Y
Rp2tm1.2Asw/Y *

Contributing Projects:
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
The Jackson Laboratory