Symbol Name ID |
Prcd
photoreceptor disc component MGI:3649529 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Attenuation of retinal blood vessels |
Optic disc pallor |
Macular degeneration |
Bone spicule pigmentation of the retina |
Rod-cone dystrophy |
Undetectable electroretinogram |
Disease(s) Associated with PRCD | ||||||
retinitis pigmentosa 36 |
Mouse Phenotypes | vision/eye phenotype |
abnormal photoreceptor outer segment morphology |
abnormal photoreceptor outer segment disc membrane morphology |
abnormal photoreceptor outer segment diameter |
abnormal retina rod cell outer segment morphology |
retina rod cell degeneration |
abnormal retina pigment epithelium morphology |
thin retina outer nuclear layer |
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Availability | Mouse Genotype | ||||||||
Prcdtm1Vya/Prcdtm1Vya | * |
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 08/02/2024 MGI 6.24 |
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