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KDM5C (NM_004187) - lysine demethylase 5C
Lysine-Specific Demethylase 5c Isoform 1
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 preferred isoform of KDM5C protein.
View all 3 isoforms
KDM5C:
lysine-specific demethylase 5C isoform 1
Description:
This gene is a member of the SMCY homolog family and encodes a protein with one ARID domain, one JmjC domain, one JmjN domain and two PHD-type zinc fingers. The DNA-binding motifs suggest this protein is involved in the regulation of transcription and chromatin remodeling. Mutations in this gene have been associated with X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009].
- Strand
- -
- Chromosome
- X
- Protein
- 1560 residues
- All mutations
- 166
- PTM sites
- 46
- CDS
- 53,222,148 - 53,254,071
- Transcription
- 53,220,502 - 53,254,604
External references
Mappings retrieved from NCBI & UniProt.