BTG1
Protein BTG1
Also known as: APRO2, BTG1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P62324
- Gene
- BTG1
- Ensembl
- ENSG00000133639
- Chromosome
- 12
- Canonical length
- 171 aa
- Protein class
- Cancer-related genes, Disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene is a member of an anti-proliferative gene family that regulates cell growth and differentiation. Expression of this gene is highest in the G0/G1 phases of the cell cycle and downregulated when cells progressed through G1. The encoded protein interacts with several nuclear receptors, and functions as a coactivator of cell differentiation. This locus has been shown to be involved in a t(8;12)(q24;q22) chromosomal translocation in a case of B-cell chronic lymphocytic leukemia. [provided by RefSeq, Oct 2008]
Canonical amino-acid sequenceUniProt
171 residues, UniProt reviewed canonical sequence.
>P62324|BTG1
1 MHPFYTRAAT MIGEIAAAVS FISKFLRTKG LTSERQLQTF SQSLQELLAE HYKHHWFPEK
61 PCKGSGYRCI RINHKMDPLI GQAAQRIGLS SQELFRLLPS ELTLWVDPYE VSYRIGEDGS
121 ICVLYEASPA GGSTQNSTNV QMVDSRISCK EELLLGRTSP SKNYNMMTVS GLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BTG1 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)
- 0.39
- Highest tissue expression
- 89 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 89 nTPM
- lymph node: 22 nTPM
- spleen: 22 nTPM
- skin: 21 nTPM
- appendix: 19 nTPM
- thymus: 19 nTPM
Single-cell type
- t-cells: 2,533 nCPM
- b-cells: 2,094 nCPM
- neutrophils: 2,082 nCPM
- innate lymphoid cells: 1,945 nCPM
- basal keratinocytes: 1,806 nCPM
- nk-cells: 1,736 nCPM
Immune cell
- eosinophil: 152 nTPM
- naive CD4 T-cell: 134 nTPM
- naive B-cell: 106 nTPM
- memory B-cell: 93 nTPM
- neutrophil: 76 nTPM
- NK-cell: 69 nTPM
Brain region
- cerebellum: 74 nTPM
- hypothalamus: 16 nTPM
- cerebral cortex: 15 nTPM
- medulla oblongata: 14 nTPM
- pons: 13 nTPM
- spinal cord: 13 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)
- 0.74
- gnomAD pLI
- 0.54
- gnomAD missense Z
- 1.36
- DepMap mean gene effect
- -0.11
- 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
- cell migration
- cell population proliferation
- negative regulation of cell growth
- negative regulation of cell population proliferation
- positive regulation of angiogenesis
- positive regulation of endothelial cell differentiation
- positive regulation of fibroblast apoptotic process
- positive regulation of myoblast differentiation
- regulation of DNA-templated transcription
- response to oxidative stress
- response to peptide hormone
- spermatogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BTG1 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 BTG1 as an antibody target. Whether an autoantibody or antibody against BTG1 could matter depends on whether native BTG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BTG1 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 BTG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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