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Symbol
Name
ID
Rpe65
retinal pigment epithelium 65
MGI:98001
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Rpe65rd12/Rpe65rd12
Rpe65tm1Lrcb/Rpe65tm1Lrcb
Rpe65tm1Tmr/Rpe65tm1Tmr
Rpe65tvrm148/Rpe65tvrm148

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