Profilin 1 - CISMeF

Preferred Label : Profilin 1;

Symbol : PFN1;

CISMeF acronym : PFN1;

Type : Gene;

Ensembl ID : ENSG00000108518;

Prefixed ID : *176610;

Details

Origin ID

176610;

UMLS CUI

C1456390;

Automatic exact mappings (from CISMeF team)
- PFN1 Gene [NCIt concept]
- PRF1 wt Allele [NCIt concept]
- profilin 1 [ORDO Gene]
- profilin 1 [HGNC gene]
- profilin 1 [MeSH concept]
- profilins [MeSH Descriptor]
HGNC gene
- profilin 1 [HGNC gene]
NCIt concept(s)
- PFN1 Gene [NCIt concept]
- PFN1 wt Allele [NCIt concept]
- Profilin-1 [NCIt concept]
ORDO concept(s)
- profilin 1 [ORDO Gene]
Phenotypes related
- Amyotrophic lateral sclerosis 18 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PFN1 Gene [NCIt concept]
- profilin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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