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 NLocalizationUniProt · 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: AutoantibodyPubMed
8 publications
- The relationship of parietal cell, gastrin cell, and thyroid autoantibodies to the state of the gastric mucosa in a population sample.
1984 · Scand J Gastroenterol · RCR 1.1 · 23 citations - Autoantibody to the gastrin receptor in pernicious anemia.
1985 · N Engl J Med · RCR 0.8 · 22 citations - Demonstration of gastrin cell autoantibodies in antral gastritis with avidin-biotin complex antibody technique.
1984 · Clin Exp Immunol · RCR 0.5 · 13 citations - Gastric type I carcinoid: a pilot study with human G17DT immunogen vaccination.
2011 · Cancer Immunol Immunother · RCR 0.3 · 9 citations - [Serum gastrin in rheumatoid arthritis].
1982 · Minerva Med · RCR 0.1 · 1 citations
Show 3 more
- Autoantibodies to gastrin in patients with pernicious anaemia--a novel antibody.
1998 · QJM · RCR 0 · 1 citations - Autoantibody against diiodinated tyrosine-gastrin in a patient with Graves' disease.
1987 · Clin Chem · RCR 0 · 1 citations - [Autoantibodies to gastrin in the blood of non-immune rabbits].
1976 · Fiziol Zh SSSR Im I M Sechenova
Reference: B cellIEDB
1 publication
- Peptide microarray-based characterization of antibody responses to host proteins after bacille Calmette-Guérin vaccination.
2017 · Int J Infect Dis · RCR 0.7 · 19 citations
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.
Loading the interactive Seroatlas protein explorer...