PRSS1 wt Allele

Preferred Label : PRSS1 wt Allele;

NCIt synonyms : Trypsinogen, Cationic Gene; Protease, Serine, 1 (Trypsin 1) wt Allele; TRY1; TRY4; TRYP1; TRP1; Protease, Serine, 1 Gene;

NCIt definition : Human PRSS1 wild-type allele is located in the vicinity of 7q34 and is approximately 4 kb in length. This allele, which encodes trypsin-1 protein, plays a role in proteolysis and digestion. Mutations in this gene are associated with both hereditary pancreatitis and trypsinogen deficiency.;

GenBank Accession Number : NM_002769;

Details

Origin ID

C113758;

UMLS CUI

C3811247;

Automatic exact mappings (from CISMeF team)
- Protease, serine, 1 [OMIM gene]
- Protease, serine, 3 [OMIM gene]
- Transient receptor potential cation channel, subfamily C, member 1 [OMIM gene]
- Trna proline (anticodon agg) 2-5 [OMIM gene]
- serine endopeptidases [MeSH Descriptor]
- serine protease 1 [ORDO Gene]
- serine proteases [MeSH Descriptor]
OMIM relation
- Protease, serine, 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 7q34 [NCIt concept]
gene_is_element_in_pathway
- Neuroactive Ligand-Receptor Signaling Pathway [NCIt concept]
gene_plays_role_in_process
- Digestion [NCIt concept]
- Hydrolysis [NCIt concept]
- Protein Degradation Induction [NCIt concept]
- Proteolysis [NCIt concept]

Keyword's position in hierarchy(ies) :

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