CYLD - Gene browser

CYLD

CYLD lysine 63 deubiquitinase

HCNC Approved Symbol: CYLD (HGNC:2584)
Genomic Coordinates: 16:50,742,086 - 50,801,935 (16q12.1)
Synonyms: KIAA0849, USPL2, CYLD1
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

4Patients

In total, 4 patients were diagnosed with a variant in the CYLD gene.

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

04
Patient count

Basal cell carcinoma: 2 (50.0%)
Patient Count: 2 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (50.0%)
Facial angiofibromas: 2 (50.0%)
Patient Count: 2 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (50.0%)
Phenotypic abnormality: 2 (50.0%)
Patient Count: 2 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (50.0%)
Elevated serum alanine aminotransferase: 1 (25.0%)
Patient Count: 1 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (25.0%)
Elevated serum aspartate aminotransferase: 1 (25.0%)
Patient Count: 1 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (25.0%)