PTGDS wt Allele

Preferred Label : PTGDS wt Allele;

NCIt synonyms : PGDS2; Prostaglandin D2 Synthase wt Allele; LPGDS; PDS; Prostaglandin D2 Synthase, Brain Gene; Prostaglandin D2 Synthase (21kD, Brain) Gene; Prostaglandin D Synthase, Lipocalin-Type Gene; Prostaglandin D2 Synthase 21kDa (Brain) Gene; PGD2; PGDS; L-PGDS;

NCIt definition : Human PTGDS wild-type allele is located in the vicinity of 9q34.3 and is approximately 7 kb in length. This allele, which encodes prostaglandin-H2 D-isomerase protein, plays a role in prostaglandin metabolism.;

NCI Metathesaurus CUI : CL951197;

GenBank Accession Number : AA621632;

Details

Origin ID

C159267;

UMLS CUI

C5202748;

Automatic exact mappings (from CISMeF team)
- After-Hours care [MeSH Descriptor]
- Ocular pigment dispersion with or without glaucoma [OMIM Phenotype]
- Pendred syndrome [OMIM Phenotype]
- Prostaglandin D synthase, hematopoietic [OMIM gene]
- Prostaglandin D2 [LOINC component]
- Prostaglandin d2 synthase, brain [OMIM gene]
- prostaglandin d2 [MeSH Descriptor]
- solute carrier family 26 member 4 [ORDO Gene]
False automatic mappings
- Contact with health services for preimplantation genetic diagnosis [ICD-11 More detail]
OMIM relation
- Prostaglandin d2 synthase, brain [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 9q34.3 [NCIt concept]
gene_is_element_in_pathway
- Arachidonic Acid Metabolism Pathway [NCIt concept]
gene_plays_role_in_process
- Lipid Binding [NCIt concept]
- Oxidation/Reduction [NCIt concept]
- Prostaglandin Production [NCIt concept]

Keyword's position in hierarchy(ies) :

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