Gene Symbol:
RPE65
HGNC:10294
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
1p31.3
Filters:

Definitive classifications

Leber congenital amaurosis 9
Submitted as: OMIM:608553
AR
07/22/2015
Evaluated
09/11/2023
Submitted
Leber congenital amaurosis 2
Submitted as: OMIM:204100
AR
04/25/2017
Evaluated
09/11/2023
Submitted
RPE65-related recessive retinopathy
AR
05/24/2022
Evaluated
04/21/2024
Submitted

Strong classifications

Leber congenital amaurosis 2
Submitted as: OMIM:204100
AR
06/08/2023
Evaluated
11/30/2023
Submitted
retinitis pigmentosa 20
Submitted as: OMIM:613794
AR
05/24/2023
Evaluated
11/30/2023
Submitted
RPE65-related dominant retinopathy
AD
02/07/2022
Evaluated
04/21/2024
Submitted

Supportive classifications

retinitis pigmentosa
Submitted as: Orphanet:791
AD
09/14/2021
Evaluated
09/14/2021
Submitted
Leber congenital amaurosis
Submitted as: Orphanet:65
AD
09/14/2021
Evaluated
09/14/2021
Submitted
severe early-childhood-onset retinal dystrophy
Submitted as: Orphanet:364055
AR
09/14/2021
Evaluated
09/14/2021
Submitted

The GenCC data are available free of restriction under a CC0 1.0 Universal (CC0 1.0) Public Domain Dedication. The GenCC requests that you give attribution to GenCC and the contributing sources whenever possible and appropriate. The accepted Flagship manuscript is now available from Genetics in Medicine (https://www.gimjournal.org/article/S1098-3600(22)00746-8/fulltext).

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. The GenCC does not independently verify the submitted information. Though the information is obtained from sources believed to be reliable, no warranty, expressed or implied, is made regarding accuracy, adequacy, completeness, reliability or usefulness of any information. This disclaimer applies to both isolated and aggregate uses of the information. The information is provided on an "as is" basis, collected through periodic submission and therefore may not represent the most up-to-date information from the submitters. If you have questions about the medical relevance of information contained on this website, please see a healthcare professional; if you have questions about specific gene-disease claims, please contact the relevant sources; and if you have questions about the representation of the data on this website, please contact gencc@thegencc.org.