TRH wt Allele - CISMeF

Preferred Label : TRH wt Allele;

NCIt synonyms : Pro-TRH Gene; TRH; Thyrotropin-Releasing Hormone Gene; Thyrotropin Releasing Hormone wt Allele;

NCIt definition : Human TRH wild-type allele is located within 3q13.3-q21 and is approximately 3 kb in length. This allele, which encodes pro-thyrotropin-releasing hormone protein, plays a role in the regulation of both thyroid function and neurotransmission. Decreased expression of this gene can result in hypothyroidism.;

GenBank Accession Number : NM_007117;

Details

Origin ID

C52432;

UMLS CUI

C1705225;

Automatic exact mappings (from CISMeF team)
- TRH [LOINC component]
- Thyrotropin releasing factor [OBSOLETE LOINC component]
- Thyrotropin releasing factor (substance) [SNOMED CT concept]
- Thyrotropin releasing hormone [LOINC component]
- Thyrotropin-releasing hormone [OMIM gene]
- pyroglutaminyl-seryl-leucinamide [MeSH Supplementary Concept]
- thyrotropin releasing hormone [ORDO Gene]
- thyrotropin-releasing hormone [MeSH Descriptor]
OMIM relation
- Thyrotropin-releasing hormone [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 3q13.3-q21 [NCIt concept]
gene_plays_role_in_process
- Intercellular Communication Process [NCIt concept]
- Neuronal Transmission [NCIt concept]
- Protein Secretion [NCIt concept]

Keyword's position in hierarchy(ies) :

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