STAP2
Signal-transducing adaptor protein 2
Also known as: BKS, STAP-2, STAP2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UGK3
- Gene
- STAP2
- Ensembl
- ENSG00000178078
- Chromosome
- 19
- Canonical length
- 403 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes the substrate of breast tumor kinase, an Src-type non-receptor tyrosine kinase. The encoded protein possesses domains and several tyrosine phosphorylation sites characteristic of adaptor proteins that mediate the interactions linking proteins involved in signal transduction pathways. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
403 residues, UniProt reviewed canonical sequence.
>Q9UGK3|STAP2
1 MASALRPPRV PKPKGVLPSH YYESFLEKKG PCDRDYKKFW AGLQGLTIYF YNSNRDFQHV
61 EKLNLGAFEK LTDEIPWGSS RDPGTHFSLI LRDQEIKFKV ETLECREMWK GFILTVVELR
121 VPTDLTLLPG HLYMMSEVLA KEEARRALET PSCFLKVSRL EAQLLLERYP ECGNLLLRPS
181 GDGADGVSVT TRQMHNGTHV VRHYKVKREG PKYVIDVEQP FSCTSLDAVV NYFVSHTKKA
241 LVPFLLDEDY EKVLGYVEAD KENGENVWVA PSAPGPGPAP CTGGPKPLSP ASSQDKLPPL
301 PPLPNQEENY VTPIGDGPAV DYENQDVASS SWPVILKPKK LPKPPAKLPK PPVGPKPEPK
361 VFNGGLGRKL PVSSAQPLFP TAGLADMTAE LQKKLEKRRA LEHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against STAP2 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)
- 0.48
- Highest tissue expression
- 90 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 90 nTPM
- duodenum: 73 nTPM
- skin: 72 nTPM
- colon: 68 nTPM
- small intestine: 68 nTPM
- rectum: 56 nTPM
Single-cell type
- enterocytes: 425 nCPM
- esophageal apical cells: 379 nCPM
- colonocytes: 356 nCPM
- esophageal suprabasal cells: 290 nCPM
- enteric transient amplifying cells: 178 nCPM
- esophageal basal cells: 160 nCPM
Immune cell
- NK-cell: 8 nTPM
- T-reg: 2.5 nTPM
- MAIT T-cell: 2.3 nTPM
- naive CD4 T-cell: 2.3 nTPM
- plasmacytoid DC: 2.2 nTPM
- naive CD8 T-cell: 1.4 nTPM
Brain region
- cerebellum: 4.6 nTPM
- choroid plexus: 4.4 nTPM
- cerebral cortex: 3.4 nTPM
- basal ganglia: 2.6 nTPM
- pons: 2.5 nTPM
- amygdala: 2.4 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)
- 1.43
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.6
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of STAP2 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 STAP2 as an antibody target. Whether an autoantibody or antibody against STAP2 could matter depends on whether native STAP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
STAP2 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 STAP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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