Symbol Name ID |
Rpe65
retinal pigment epithelium 65 MGI:98001 |
Darker colors indicate more annotations |
Human Phenotypes | Photophobia |
Cerebellar vermis hypoplasia |
Eye poking |
Intellectual disability |
Hyperreflexia |
Disease(s) Associated with RPE65 | |||||
Leber congenital amaurosis 2 | |||||
retinitis pigmentosa |
Mouse Phenotypes | short photoreceptor inner segment |
abnormal photoreceptor outer segment morphology |
short photoreceptor outer segment |
abnormal retina rod cell outer segment morphology |
disorganized photoreceptor outer segment |
photoreceptor outer segment degeneration |
retina cone cell degeneration |
retina rod cell degeneration |
retina photoreceptor degeneration |
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Availability | Mouse Genotype | |||||||||
Rpe65rd12/Rpe65rd12 | ||||||||||
Rpe65tm1Lrcb/Rpe65tm1Lrcb | ||||||||||
Rpe65tm1Tmr/Rpe65tm1Tmr | ||||||||||
Rpe65tvrm148/Rpe65tvrm148 |
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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