Seroatlas · Human Serome Atlas

GAST

Gastrin

Also known as: GAS, GAST_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P01350
Gene
GAST
Ensembl
ENSG00000184502
Chromosome
17
Canonical length
101 aa
Protein class
Cancer-related genes, FDA approved drug targets, Predicted secreted proteins
Secretome location
Secreted to digestive system

OverviewNCBI Gene

Gastrin is a hormone whose main function is to stimulate secretion of hydrochloric acid by the gastric mucosa, which results in gastrin formation inhibition. This hormone also acts as a mitogenic factor for gastrointestinal epithelial cells. Gastrin has two biologically active peptide forms, G34 and G17. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

101 residues, UniProt reviewed canonical sequence.

>P01350|GAST
     1  MQRLCVYVLI FALALAAFSE ASWKPRSQQP DAPLGTGANR DLELPWLEQQ GPASHHRRQL
    61  GPQGPPHLVA DPSKKQGPWL EEEEEAYGWM DFGRRSAEDE N

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against GAST 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
Secreted
Secreted
Yes
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.67
Highest tissue expression
9,038 nTPM

Expression across tissuesHPA

Tissue

  • stomach: 9,038 nTPM
  • duodenum: 54 nTPM
  • spleen: 8.8 nTPM
  • thymus: 4 nTPM
  • placenta: 3.9 nTPM
  • lung: 3.4 nTPM

Single-cell type

  • neuroendocrine cells: 383 nCPM
  • endometrial glandular cells: 171 nCPM
  • endometrial stromal cells: 23 nCPM
  • endometrial luminal cells: 18 nCPM
  • foveolar cells: 14 nCPM
  • syncytiotrophoblasts: 13 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • hypothalamus: 4.7 nTPM
  • midbrain: 1.4 nTPM
  • pons: 1.4 nTPM
  • amygdala: 1.3 nTPM
  • basal ganglia: 1.1 nTPM
  • cerebral cortex: 1.1 nTPM

ReferencesPubMed · IEDB

Publications for GAST from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.

Reference: B cellIEDB

1 publication

Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. IEDB — curated epitope assays from the Immune Epitope Database (Vita et al., Nucleic Acids Research 2019). Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.

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)
1.71
gnomAD pLI
0
gnomAD missense Z
0.05
DepMap mean gene effect
0
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads GAST as an antibody target. Whether an autoantibody or antibody against GAST could matter depends on whether native GAST is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

GAST is annotated as secreted, so native GAST circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.

Annotation status

The present source text does not explicitly label GAST as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/GAST. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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