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CYLD (NM_001042355) - CYLD lysine 63 deubiquitinase
Ubiquitin Carboxyl-Terminal Hydrolase Cyld Isoform 2
Legend
Mutation impacts
direct
network-rewiring
motif-changing
proximal
distal
none
Sites
multiple types
acetylation
methylation
succinylation
sumoylation
ubiquitination
glycosylation
- C-linked
- N-linked
- O-linked
- S-linked
phosphorylation
- SARS-CoV-2
Others
Exact position of a PTM site
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Mutations Visualisation
Protein summary
This is an alternative isoform of CYLD protein.
View all 3 isoforms
CYLD:
ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
Description:
This gene is encodes a cytoplasmic protein with three cytoskeletal-associated protein-glycine-conserved (CAP-GLY) domains that functions as a deubiquitinating enzyme. Mutations in this gene have been associated with cylindromatosis, multiple familial trichoepithelioma, and Brooke-Spiegler syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008].
- Strand
- +
- Chromosome
- 16
- Protein
- 953 residues
- All mutations
- 107
- PTM sites
- 45
- CDS
- 50,783,609 - 50,830,419
- Transcription
- 50,775,960 - 50,835,846
External references
Mappings retrieved from NCBI & UniProt.