CCNDBP1
Cyclin-D1-binding protein 1
Also known as: CCDB1_HUMAN, DIP1, GCIP, HHM
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95273
- Gene
- CCNDBP1
- Ensembl
- ENSG00000166946
- Chromosome
- 15
- Canonical length
- 360 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
This gene was identified by the interaction of its gene product with Grap2, a leukocyte-specific adaptor protein important for immune cell signaling. The protein encoded by this gene was shown to interact with cyclin D. Transfection of this gene in cells was reported to reduce the phosphorylation of Rb gene product by cyclin D-dependent protein kinase, and inhibit E2F1-mediated transcription activity. This protein was also found to interact with helix-loop-helix protein E12 and is thought to be a negative regulator of liver-specific gene expression. Several alternatively spliced variants have been found for this gene. [provided by RefSeq, Apr 2009]
Canonical amino-acid sequenceUniProt
360 residues, UniProt reviewed canonical sequence.
>O95273|CCNDBP1
1 MASATAPAAA VPTLASPLEQ LRHLAEELRL LLPRVRVGEA QETTEEFNRE MFWRRLNEAA
61 VTVSREATTL TIVFSQLPLP SPQETQKFCE QVHAAIKAFI AVYYLLPKDQ GITLRKLVRG
121 ATLDIVDGMA QLMEVLSVTP TQSPENNDLI SYNSVWVACQ QMPQIPRDNK AAALLMLTKN
181 VDFVKDAHEE MEQAVEECDP YSGLLNDTEE NNSDNHNHED DVLGFPSNQD LYWSEDDQEL
241 IIPCLALVRA SKACLKKIRM LVAENGKKDQ VAQLDDIVDI SDEISPSVDD LALSIYPPMC
301 HLTVRINSAK LVSVLKKALE ITKASHVTPQ PEDSWIPLLI NAIDHCMNRI KELTQSELELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCNDBP1 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
- 19 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 19 nTPM
- cerebellum: 6.6 nTPM
- adipose tissue: 3.6 nTPM
- spleen: 3.1 nTPM
- skin: 2.9 nTPM
- blood vessel: 2.6 nTPM
Single-cell type
- syncytiotrophoblasts: 1,449 nCPM
- esophageal apical cells: 536 nCPM
- cytotrophoblasts: 415 nCPM
- migrating cytotrophoblasts: 305 nCPM
- neutrophils: 270 nCPM
- platelets: 162 nCPM
Immune cell
- basophil: 22 nTPM
- non-classical monocyte: 9.5 nTPM
- T-reg: 8.4 nTPM
- neutrophil: 6.2 nTPM
- naive CD8 T-cell: 5.9 nTPM
- eosinophil: 5.6 nTPM
Brain region
- cerebellum: 8.8 nTPM
- cerebral cortex: 6.1 nTPM
- hypothalamus: 6.1 nTPM
- pons: 6.1 nTPM
- white matter: 5.9 nTPM
- basal ganglia: 5.7 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)
- 0.8
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.33
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- none
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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cyclin-D1-binding protein 1-like
- Cyclin-D1-binding protein 1-like, N-terminal
- Cyclin-D1-binding protein 1-like, C-terminal
- Grap2 and cyclin-D-interacting, N-terminal
- Grap2 and cyclin-D-interacting, C-terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CCNDBP1 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 CCNDBP1 as an antibody target. Whether an autoantibody or antibody against CCNDBP1 could matter depends on whether native CCNDBP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCNDBP1 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 CCNDBP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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