BTG4
Protein BTG4
Also known as: APRO3, BTG4_HUMAN, PC3B
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NY30
- Gene
- BTG4
- Ensembl
- ENSG00000137707
- Chromosome
- 11
- Canonical length
- 223 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Endoplasmic reticulum,Golgi apparatus
OverviewNCBI Gene
The protein encoded by this gene is a member of the BTG/Tob family. This family has structurally related proteins that appear to have antiproliferative properties. This encoded protein can induce G1 arrest in the cell cycle. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
223 residues, UniProt reviewed canonical sequence.
>Q9NY30|BTG4
1 MRDEIATTVF FVTRLVKKHD KLSKQQIEDF AEKLMTILFE TYRSHWHSDC PSKGQAFRCI
61 RINNNQNKDP ILERACVESN VDFSHLGLPK EMTIWVDPFE VCCRYGEKNH PFTVASFKGR
121 WEEWELYQQI SYAVSRASSD VSSGTSCDEE SCSKEPRVIP KVSNPKSIYQ VENLKQPFQS
181 WLQIPRKKNV VDGRVGLLGN TYHGSQKHPK CYRPAMHRLD RILLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BTG4 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)
- 0.47
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- testis: 21 nTPM
- choroid plexus: 4.2 nTPM
- fallopian tube: 1.4 nTPM
- lung: 0.4 nTPM
- pancreas: 0.1 nTPM
- thymus: 0.1 nTPM
Single-cell type
- late spermatids: 280 nCPM
- late primary spermatocytes: 147 nCPM
- early spermatids: 115 nCPM
- respiratory ciliated cells: 55 nCPM
- early primary spermatocytes: 34 nCPM
- ependymal cells: 31 nCPM
Immune cell
- T-reg: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- choroid plexus: 11 nTPM
- midbrain: 2 nTPM
- medulla oblongata: 1.4 nTPM
- pons: 0.9 nTPM
- spinal cord: 0.7 nTPM
- hippocampal formation: 0.4 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about BTG4.
Disease | AllUniProt
Conditions BTG4 is implicated in, by any mechanism.
- Oocyte/zygote/embryo maturation arrest 8 (OZEMA8) MIM:619009
Disease | GeneticClinVar
5 pathogenic / likely-pathogenic of 39 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Oocyte maturation defect 8
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
- 0.17
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- 0.11
- 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
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
InteractionsUniProt · HPA
Protein binding partners of BTG4 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 BTG4 as an antibody target. Whether an autoantibody or antibody against BTG4 could matter depends on whether native BTG4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BTG4 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 BTG4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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