Forkhead box p1

Preferred Label : Forkhead box p1;

Symbol : FOXP1;

CISMeF acronym : FOXP1;

Type : Gene;

Alternative titles and symbols : Glutamine-rich factor 1; QRF1;

Ensembl ID : ENSG00000114861;

Prefixed ID : *605515;

Details

Origin ID

605515;

UMLS CUI

C1414688;

Automatic exact mappings (from CISMeF team)
- FOXP1 wt Allele [NCIt concept]
- Forkhead Box Protein P1 [NCIt concept]
Currated CISMeF NLP mapping
- FOXP1 Gene [NCIt concept]
- forkhead box P1 [ORDO Gene]
- forkhead box P1 [HGNC gene]
HGNC gene
- forkhead box P1 [HGNC gene]
NCIt concept(s)
- FOXP1 Gene [NCIt concept]
- FOXP1 wt Allele [NCIt concept]
- Forkhead Box Protein P1 [NCIt concept]
ORDO concept(s)
- forkhead box P1 [ORDO Gene]
Phenotypes related
- Intellectual developmental disorder with language impairment and with or without autistic features [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FOXP1 Gene [NCIt concept]
- forkhead box P1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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