Symbol Name ID |
Impg2
interphotoreceptor matrix proteoglycan 2 MGI:3044955 |
Darker colors indicate more annotations |
Human Phenotypes | Attenuation of retinal blood vessels |
Abnormality of the eye |
Posterior subcapsular cataract |
Nuclear cataract |
Iris hypopigmentation |
Choroidal neovascularization |
Choroideremia |
Optic disc pallor |
Cystoid macular degeneration |
Macular atrophy |
Macular dystrophy |
Vitelliform-like macular lesions |
Pigmentary retinopathy |
Bone spicule pigmentation of the retina |
Retinal pigment epithelial atrophy |
Retinal nonattachment |
Rod-cone dystrophy |
Subretinal fluid |
Drusen |
Posterior staphyloma |
Decreased Arden ratio of electrooculogram |
Abnormal electroretinogram |
Abnormality of vision |
Color vision defect |
Metamorphopsia |
Nyctalopia |
Photophobia |
Visual impairment |
Reduced visual acuity |
Moderately reduced visual acuity |
Visual field defect |
Central scotoma |
Disease(s) Associated with IMPG2 | ||||||||||||||||||||||||||||||||
retinitis pigmentosa 56 | ||||||||||||||||||||||||||||||||
vitelliform macular dystrophy |
Mouse Phenotypes | decreased retina cone cell number |
abnormal retina rod cell inner segment morphology |
abnormal retina cone cell morphology |
retina cone cell degeneration |
abnormal retina rod cell morphology |
retina rod cell degeneration |
abnormal eye morphology |
abnormal ocular fundus morphology |
abnormal retina layer morphology |
thin retina outer nuclear layer |
retina degeneration |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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Availability | Mouse Genotype | |||||||||||||||
Impg2em1(IMPC)Mbp/Impg2em1(IMPC)Mbp | ||||||||||||||||
Impg2em1Visu/Impg2em1Visu | ||||||||||||||||
Impg2em1Xjz/Impg2em1Xjz | ||||||||||||||||
Impg2em2Xjz/Impg2em2Xjz |
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 04/09/2024 MGI 6.23 |
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