SCTR wt Allele

Preferred Label : SCTR wt Allele;

NCIt synonyms : SR; Secretin Receptor wt Allele;

NCIt definition : Human SCTR wild-type allele is located in the vicinity of 2q14.1 and is approximately 85 kb in length. This allele, which encodes secretin receptor protein plays a role in the regulation of pancreatic bicarbonate, electrolyte and volume secretion. Dysfunction of the gene may be involved in pancreatic cancer and autism.;

GenBank Accession Number : NM_002980;

Details

Origin ID

C51472;

UMLS CUI

C1705646;

Automatic exact mappings (from CISMeF team)
- Intellectual developmental disorder, X-linked, syndromic, snyder-robinson type [OMIM Phenotype]
- SR-AT [MeSH concept]
- SR-AT [MeSH Supplementary Concept]
- SRS-A [MeSH Descriptor]
- SRS-A [MeSH concept]
- Silver-russell syndrome 1 [OMIM Phenotype]
- Slow reacting substance-A of anaphylaxis (substance) [SNOMED CT concept]
- racemate [IUPAC Term]
- spermine synthase [ORDO Gene]
OMIM relation
- Secretin receptor [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_associated_with_disease
- Pancreatic Carcinoma [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 2q14.1 [NCIt concept]
gene_is_element_in_pathway
- Neuroactive Ligand-Receptor Signaling Pathway [NCIt concept]
gene_plays_role_in_process
- Digestion [NCIt concept]
- G Protein-Coupled Receptor Signaling [NCIt concept]
- Homeostatic Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Receptor Signaling [NCIt concept]
- Signal Transduction [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

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