HCST
Hematopoietic cell signal transducer
Also known as: DAP10, DKFZP586C1522, HCST_HUMAN, KAP10, PIK3AP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UBK5
- Gene
- HCST
- Ensembl
- ENSG00000126264
- Chromosome
- 19
- Canonical length
- 93 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Golgi apparatus,Vesicles,Plasma membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a transmembrane signaling adaptor that contains a YxxM motif in its cytoplasmic domain. The encoded protein may form part of the immune recognition receptor complex with the C-type lectin-like receptor NKG2D. As part of this receptor complex, this protein may activate phosphatidylinositol 3-kinase dependent signaling pathways through its intracytoplasmic YxxM motif. This receptor complex may have a role in cell survival and proliferation by activation of NK and T cell responses. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
93 residues, UniProt reviewed canonical sequence.
>Q9UBK5|HCST
1 MIHLGHILFL LLLPVAAAQT TPGERSSLPA FYPGTSGSCS GCGSLSLPLL AGLVAADAVA
61 SLLIVGAVFL CARPRRSPAQ EDGKVYINMP GRGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HCST 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.6
- Highest tissue expression
- 239 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 239 nTPM
- spleen: 113 nTPM
- lymph node: 64 nTPM
- thymus: 56 nTPM
- appendix: 51 nTPM
- choroid plexus: 50 nTPM
Single-cell type
- hofbauer cells: 856 nCPM
- nk-cells: 726 nCPM
- t-cells: 546 nCPM
- cdc: 396 nCPM
- monocytes: 365 nCPM
- platelets: 349 nCPM
Immune cell
- gdT-cell: 1,588 nTPM
- total PBMC: 1,424 nTPM
- NK-cell: 1,295 nTPM
- memory CD8 T-cell: 1,294 nTPM
- MAIT T-cell: 1,175 nTPM
- naive CD8 T-cell: 1,112 nTPM
Brain region
- white matter: 28 nTPM
- thalamus: 20 nTPM
- medulla oblongata: 19 nTPM
- spinal cord: 17 nTPM
- hypothalamus: 17 nTPM
- choroid plexus: 16 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)
- 1.79
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.48
- DepMap mean gene effect
- -0.05
- 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
- natural killer cell mediated cytotoxicity
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- protein phosphorylation
- regulation of immune response
Molecular functions
- phosphatidylinositol 3-kinase binding
- protein-macromolecule adaptor activity
- signaling receptor binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Hematopoietic cell signal transducer
- DAP10 membrane protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HCST 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 HCST as an antibody target. Whether an autoantibody or antibody against HCST could matter depends on whether native HCST is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HCST is annotated at the cell surface, where native HCST is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label HCST as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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