CDC6
Cell division control protein 6 homolog
Also known as: CDC18L, CDC6_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99741
- Gene
- CDC6
- Ensembl
- ENSG00000094804
- Chromosome
- 17
- Canonical length
- 560 aa
- Protein class
- Cancer-related genes, Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytokinetic bridge,Mitotic spindle,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Cdc6, a protein essential for the initiation of DNA replication. This protein functions as a regulator at the early steps of DNA replication. It localizes in cell nucleus during cell cyle G1, but translocates to the cytoplasm at the start of S phase. The subcellular translocation of this protein during cell cyle is regulated through its phosphorylation by Cdks. Transcription of this protein was reported to be regulated in response to mitogenic signals through transcriptional control mechanism involving E2F proteins. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
560 residues, UniProt reviewed canonical sequence.
>Q99741|CDC6
1 MPQTRSQAQA TISFPKRKLS RALNKAKNSS DAKLEPTNVQ TVTCSPRVKA LPLSPRKRLG
61 DDNLCNTPHL PPCSPPKQGK KENGPPHSHT LKGRRLVFDN QLTIKSPSKR ELAKVHQNKI
121 LSSVRKSQEI TTNSEQRCPL KKESACVRLF KQEGTCYQQA KLVLNTAVPD RLPAREREMD
181 VIRNFLREHI CGKKAGSLYL SGAPGTGKTA CLSRILQDLK KELKGFKTIM LNCMSLRTAQ
241 AVFPAIAQEI CQEEVSRPAG KDMMRKLEKH MTAEKGPMIV LVLDEMDQLD SKGQDVLYTL
301 FEWPWLSNSH LVLIGIANTL DLTDRILPRL QAREKCKPQL LNFPPYTRNQ IVTILQDRLN
361 QVSRDQVLDN AAVQFCARKV SAVSGDVRKA LDVCRRAIEI VESDVKSQTI LKPLSECKSP
421 SEPLIPKRVG LIHISQVISE VDGNRMTLSQ EGAQDSFPLQ QKILVCSLML LIRQLKIKEV
481 TLGKLYEAYS KVCRKQQVAA VDQSECLSLS GLLEARGILG LKRNKETRLT KVFFKIEEKE
541 IEHALKDKAL IGNILATGLPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CDC6 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 26 nTPM
- tonsil: 16 nTPM
- thymus: 16 nTPM
- lymph node: 15 nTPM
- appendix: 13 nTPM
- testis: 9.4 nTPM
Single-cell type
- early primary spermatocytes: 120 nCPM
- erythrocyte progenitors: 69 nCPM
- oocytes: 60 nCPM
- extravillous trophoblasts: 40 nCPM
- megakaryocyte progenitors: 39 nCPM
- migrating cytotrophoblasts: 36 nCPM
Immune cell
- plasmacytoid DC: 3.6 nTPM
- T-reg: 2.4 nTPM
- NK-cell: 1.5 nTPM
- memory CD8 T-cell: 1.1 nTPM
- naive CD8 T-cell: 1.1 nTPM
- gdT-cell: 0.8 nTPM
Brain region
- cerebral cortex: 5.4 nTPM
- basal ganglia: 3.2 nTPM
- white matter: 3 nTPM
- amygdala: 2.7 nTPM
- pons: 2.6 nTPM
- hippocampal formation: 2.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CDC6.
Disease | AllUniProt
Conditions CDC6 is implicated in, by any mechanism.
- Meier-Gorlin syndrome 5 (MGORS5) MIM:613805
Disease | ImmuneIEDB
Conditions an epitope on CDC6 was assayed in.
- invasive ductal carcinoma T cell
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.61
- DepMap mean gene effect
- -1.36
- DepMap dependency class
- pan
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell division
- cellular response to angiotensin
- cellular response to vasopressin
- DNA replication checkpoint signaling
- DNA replication initiation
- mitotic DNA replication checkpoint signaling
- negative regulation of cell population proliferation
- negative regulation of DNA replication
- positive regulation of chromosome segregation
- positive regulation of cytokinesis
- positive regulation of fibroblast proliferation
- regulation of cyclin-dependent protein serine/threonine kinase activity
- regulation of mitotic metaphase/anaphase transition
- traversing start control point of mitotic cell cycle
Molecular functions
- ATP binding
- chromatin binding
- DNA replication origin binding
- nucleotide binding
- protein serine/threonine kinase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- AAA+ ATPase domain
- Cdc6, C-terminal
- P-loop containing nucleoside triphosphate hydrolase
- Winged helix-like DNA-binding domain superfamily
- Winged helix DNA-binding domain superfamily
- Orc1-like, AAA ATPase domain
- Origin recognition complex 1/Cell division control protein 6
- CDC6, C terminal winged helix domain
- AAA ATPase domain
- Cell division protein Cdc6/18
- Cdc6/ORC1-like, ATPase lid domain
- Cdc6/ORC-like, ATPase lid domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CDC6 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CDC6 as an antibody target. Whether an autoantibody or antibody against CDC6 could matter depends on whether native CDC6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CDC6 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CDC6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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