UCHL1 - Gene browser | 3billion

UCHL1

UCHL1

ubiquitin C-terminal hydrolase L1

HCNC Approved Symbol: UCHL1 (HGNC:12513)
Genomic Coordinates: 4:41,256,928 - 41,268,455 (4p13)
Synonyms: PGP9.5, Uch-L1, UCHL-1, PARK5
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the UCHL1 gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

01
Patient count

Gait disturbance: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Optic atrophy: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Spastic paraparesis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

UCHL1 - Gene browser | 3billion