Forkhead box g1

Preferred Label : Forkhead box g1;

Symbol : FOXG1;

CISMeF acronym : FOXG1;

Type : Gene;

Alternative titles and symbols : Forkhead box g1b; Forkhead-like 1; Oncogene qin; Brain factor 1; FOXG1B; FKHL1; BF1;

Ensembl ID : ENSG00000176165;

Prefixed ID : *164874;

Details

Origin ID

164874;

UMLS CUI

C0812297;

Automatic exact mappings (from CISMeF team)
- FOXG1 Gene [NCIt concept]
- FOXG1 wt Allele [NCIt concept]
- Forkhead Box Protein G1 [NCIt concept]
- forkhead box G1 [ORDO Gene]
- forkhead box G1 [HGNC gene]
HGNC gene
- forkhead box G1 [HGNC gene]
NCIt concept(s)
- FOXG1 Gene [NCIt concept]
- FOXG1 wt Allele [NCIt concept]
- Forkhead Box Protein G1 [NCIt concept]
ORDO concept(s)
- forkhead box G1 [ORDO Gene]
Phenotypes related
- Rett syndrome, congenital variant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FOXG1 Gene [NCIt concept]
- forkhead box G1 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients