FOXP2 wt Allele

Preferred Label : FOXP2 wt Allele;

NCIt synonyms : SPCH1; Forkhead Box P2 wt Allele; CAGH44; TNRC10; DKFZp686H1726;

NCIt definition : Human FOXP2 wild-type allele is located in the vicinity of 7q31 and is approximately 279 kb in length. This allele, which encodes forkhead box protein P2, plays a role in transcription during brain development. Mutations in the gene are associated with speech-language disorder 1 and a translocation t(5;7)(q22;q31.2) is associated with severe speech and language impairment.;

GenBank Accession Number : U80741;

Details

Origin ID

C75490;

UMLS CUI

C2700051;

OMIM relation
- Forkhead box p2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 7q31 [NCIt concept]
gene_plays_role_in_process
- DNA Binding [NCIt concept]
- Organogenesis [NCIt concept]
- Transcriptional Regulation [NCIt concept]
- Transcriptional Repression [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients