Gene Symbol:
UCHL1
HGNC:12513
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
4p13
Filters:

Strong classifications

spastic paraplegia 79A, autosomal dominant, with ataxia
Submitted as: OMIM:620221
AD
03/13/2023
Evaluated
11/30/2023
Submitted
early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome
Submitted as: OMIM:615491
AR
07/15/2020
Evaluated
11/30/2023
Submitted

Moderate classifications

early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome
Submitted as: OMIM:615491
AR
05/14/2018
Evaluated
12/24/2020
Submitted
spastic paraplegia 79A, autosomal dominant, with ataxia
Submitted as: OMIM:620221
AD
01/20/2023
Evaluated
08/19/2023
Submitted

Supportive classifications

early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome
Submitted as: Orphanet:352654
AR
09/14/2021
Evaluated
09/14/2021
Submitted

Limited classifications

Parkinson disease 5, autosomal dominant, susceptibility to
Submitted as: OMIM:613643
AD
10/15/2021
Evaluated
11/30/2023
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.