CDKN1B
Cyclin-dependent kinase inhibitor 1B
Also known as: CDN1B_HUMAN, KIP1, P27KIP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P46527
- Gene
- CDKN1B
- Ensembl
- ENSG00000111276
- Chromosome
- 12
- Canonical length
- 198 aa
- Protein class
- Cancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Primary cilium,Primary cilium transition zone,Centrosome,Basal body,Cytosol
OverviewNCBI Gene
This gene encodes a cyclin-dependent kinase inhibitor, which shares a limited similarity with CDK inhibitor CDKN1A/p21. The encoded protein binds to and prevents the activation of cyclin E-CDK2 or cyclin D-CDK4 complexes, and thus controls the cell cycle progression at G1. The degradation of this protein, which is triggered by its CDK dependent phosphorylation and subsequent ubiquitination by SCF complexes, is required for the cellular transition from quiescence to the proliferative state. Mutations in this gene are associated with multiple endocrine neoplasia type IV (MEN4). [provided by RefSeq, Apr 2014]
Canonical amino-acid sequenceUniProt
198 residues, UniProt reviewed canonical sequence.
>P46527|CDKN1B
1 MSNVRVSNGS PSLERMDARQ AEHPKPSACR NLFGPVDHEE LTRDLEKHCR DMEEASQRKW
61 NFDFQNHKPL EGKYEWQEVE KGSLPEFYYR PPRPPKGACK VPAQESQDVS GSRPAAPLIG
121 APANSEDTHL VDPKTDPSDS QTGLAEQCAG IRKRPATDDS STQNKRANRT EENVSDGSPN
181 AGSVEQTPKK PGLRRRQTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CDKN1B 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)
- 0.66
- Highest tissue expression
- 100 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 100 nTPM
- blood vessel: 83 nTPM
- skeletal muscle: 76 nTPM
- spinal cord: 75 nTPM
- thymus: 67 nTPM
- bone marrow: 64 nTPM
Single-cell type
- neutrophils: 254 nCPM
- müller glia: 188 nCPM
- t-cells: 184 nCPM
- retinal pigment epithelial cells: 158 nCPM
- esophageal apical cells: 149 nCPM
- plasma cells: 146 nCPM
Immune cell
- neutrophil: 21 nTPM
- T-reg: 12 nTPM
- eosinophil: 8.2 nTPM
- naive CD4 T-cell: 7.6 nTPM
- memory CD4 T-cell: 7.5 nTPM
- memory CD8 T-cell: 6.9 nTPM
Brain region
- white matter: 149 nTPM
- cerebellum: 115 nTPM
- basal ganglia: 108 nTPM
- pons: 90 nTPM
- medulla oblongata: 87 nTPM
- hypothalamus: 86 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CDKN1B.
Disease | AllUniProt
Conditions CDKN1B is implicated in, by any mechanism.
- Multiple endocrine neoplasia 4 (MEN4) MIM:610755
Disease | GeneticClinVar
119 pathogenic / likely-pathogenic of 1,119 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Multiple endocrine neoplasia type 4
- Hereditary cancer-predisposing syndrome
- Neuroendocrine neoplasm
- Lung cancer
- Neoplasm
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)
- 0.65
- gnomAD pLI
- 0.62
- gnomAD missense Z
- -1.85
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- autophagic cell death
- cellular response to antibiotic
- cellular response to lithium ion
- cellular senescence
- DNA damage response, signal transduction by p53 class mediator
- epithelial cell apoptotic process
- epithelial cell proliferation involved in prostate gland development
- G1/S transition of mitotic cell cycle
- heart development
- inner ear development
- negative regulation of cardiac muscle tissue regeneration
- negative regulation of cell growth
- negative regulation of cell population proliferation
- negative regulation of epithelial cell apoptotic process
- negative regulation of epithelial cell proliferation
- negative regulation of epithelial cell proliferation involved in prostate gland development
- negative regulation of mitotic cell cycle
- negative regulation of vascular associated smooth muscle cell proliferation
- Notch signaling pathway
- nuclear export
- placenta development
- positive regulation of cell population proliferation
- positive regulation of DNA replication
- positive regulation of microtubule polymerization
- positive regulation of protein catabolic process
- potassium ion transport
- regulation of cell cycle
- regulation of cell cycle G1/S phase transition
- regulation of cell migration
- regulation of cyclin-dependent protein serine/threonine kinase activity
- regulation of exit from mitosis
- regulation of G1/S transition of mitotic cell cycle
- regulation of lens fiber cell differentiation
- sensory perception of sound
Molecular functions
- cyclin binding
- cyclin-dependent protein serine/threonine kinase inhibitor activity
- molecular adaptor activity
- molecular function inhibitor activity
- protein kinase binding
- protein kinase inhibitor activity
- protein phosphatase binding
- protein-containing complex binding
- protein-folding chaperone binding
- ubiquitin ligase activator activity
- ubiquitin protein ligase binding
- cyclin-dependent protein kinase regulator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CDKN1B 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 CDKN1B as an antibody target. Whether an autoantibody or antibody against CDKN1B could matter depends on whether native CDKN1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CDKN1B 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 CDKN1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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