PSPN wt Allele

Preferred Label : PSPN wt Allele;

NCIt synonyms : Persephin wt Allele; PSP;

NCIt definition : Human PSPN wild-type allele is located in the vicinity of 19p13.3 and is approximately 4 kb in length. This allele, which encodes persephin protein, is involved in receptor signaling and neuronal survival.;

NCI Metathesaurus CUI : CL1663688;

GenBank Accession Number : AF040962;

Détails

Origin ID

C181102;

UMLS CUI

C5551043;

Automatic exact mappings (from CISMeF team)
- Heat-responsive protein 12 [OMIM gene]
- Phenol red [ICD-11 Extension code]
- Phosphoserine phosphatase [OMIM gene]
- Pneumothorax, primary spontaneous [OMIM Phenotype]
- Progressive supranuclear ophthalmoplegia (disorder) [SNOMED CT concept]
- Regenerating islet-derived 1 alpha (pancreatic stone protein, pancreatic thread protein) [ORDO Gene]
- Supranuclear palsy, progressive, 1 [OMIM Phenotype]
- Syntaxin-binding protein 3 [OMIM gene]
- microseminoprotein beta [ORDO Gene]
- progressive supranuclear palsy [MedlinePlus Topic]
OMIM relation
- Persephin [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 19p13.3 [NCIt concept]
gene_plays_role_in_process
- Cell Proliferation Regulatory Process [NCIt concept]
- Nerve Cell Survival [NCIt concept]
- Nervous System Development [NCIt concept]
- Receptor Binding [NCIt concept]
- Receptor Signaling [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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