CCNG1
Cyclin-G1
Also known as: CCNG, CCNG1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P51959
- Gene
- CCNG1
- Ensembl
- ENSG00000113328
- Chromosome
- 5
- Canonical length
- 295 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
The eukaryotic cell cycle is governed by cyclin-dependent protein kinases (CDKs) whose activities are regulated by cyclins and CDK inhibitors. The protein encoded by this gene is a member of the cyclin family and contains the cyclin box. The encoded protein lacks the protein destabilizing (PEST) sequence that is present in other family members. Transcriptional activation of this gene can be induced by tumor protein p53. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
295 residues, UniProt reviewed canonical sequence.
>P51959|CCNG1
1 MIEVLTTTDS QKLLHQLNAL LEQESRCQPK VCGLRLIESA HDNGLRMTAR LRDFEVKDLL
61 SLTQFFGFDT ETFSLAVNLL DRFLSKMKVQ PKHLGCVGLS CFYLAVKSIE EERNVPLATD
121 LIRISQYRFT VSDLMRMEKI VLEKVCWKVK ATTAFQFLQL YYSLLQENLP LERRNSINFE
181 RLEAQLKACH CRIIFSKAKP SVLALSIIAL EIQAQKCVEL TEGIECLQKH SKINGRDLTF
241 WQELVSKCLT EYSSNKCSKP NVQKLKWIVS GRTARQLKHS YYRITHLPTI PEMVPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCNG1 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)
- 0.31
- Highest tissue expression
- 153 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 153 nTPM
- duodenum: 129 nTPM
- liver: 121 nTPM
- kidney: 115 nTPM
- tongue: 113 nTPM
- ovary: 105 nTPM
Single-cell type
- platelets: 567 nCPM
- enterocytes: 236 nCPM
- esophageal apical cells: 198 nCPM
- migrating cytotrophoblasts: 194 nCPM
- enteric transient amplifying cells: 192 nCPM
- enteric stem cells: 191 nCPM
Immune cell
- naive CD4 T-cell: 85 nTPM
- T-reg: 81 nTPM
- naive CD8 T-cell: 72 nTPM
- total PBMC: 64 nTPM
- memory CD4 T-cell: 63 nTPM
- myeloid DC: 60 nTPM
Brain region
- white matter: 40 nTPM
- choroid plexus: 40 nTPM
- medulla oblongata: 34 nTPM
- spinal cord: 32 nTPM
- hypothalamus: 31 nTPM
- cerebellum: 30 nTPM
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)
- 0.99
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.76
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell division
- G1/S transition of mitotic cell cycle
- regulation of cyclin-dependent protein serine/threonine kinase activity
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CCNG1 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 CCNG1 as an antibody target. Whether an autoantibody or antibody against CCNG1 could matter depends on whether native CCNG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCNG1 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 CCNG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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