FOXG1 wt Allele

Preferred Label : FOXG1 wt Allele;

NCIt synonyms : FKHL4; HFK2; HBF-1; FOXG1C; FKH2; HBF-3; FOXG1A; HFK1; QIN; FOXG1B Gene; FOXG1B; BF2; HBF-2; FKHL3; Forkhead Box G1 wt Allele; FKHL1; HFK3; HBF-G2; KHL2; BF1; FKHL2; Forkhead Box G1B Gene; HBF2; FOXG1B wt Allele;

NCIt definition : Human FOXG1 wild-type allele is located within 14q12-q13 and is approximately 4 kb in length. This allele, which encodes forkhead box protein G1, is involved in both the modulation of transcription by RNA polymerase II and in the regional development of the brain.;

GenBank Accession Number : NM_005249;

Details

Origin ID

C52899;

UMLS CUI

C1705148;

OMIM relation
- Forkhead box g1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 14: 28306038-28308622 [NCIt concept]
gene_in_chromosomal_location
- 14q13 [NCIt concept]
gene_plays_role_in_process
- DNA Binding [NCIt concept]
- Transcriptional Regulation [NCIt concept]
- Transcriptional Repression [NCIt concept]

Keyword's position in hierarchy(ies) :

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