FOXP2 wt Allele

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. (NCI Thesaurus)

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FOXP2 Gene

This gene is involved in brain development.

FOXP1 wt Allele

Human FOXP1 wild-type allele is located in the vicinity of 3p14.1 and is approximately 629 kb in length. This allele, which encodes…

FOXP1 Gene

This gene is involved in transcriptional modulation.

FOXO6 wt Allele

Human FOXO6 wild-type allele is located in the vicinity of 1p34.2 and is approximately 22 kb in length. This allele, which encodes…

FOXO6 Gene

This gene may play a role in transcriptional activation.

FOXO4 wt Allele

Human FOXO4 wild-type allele is located in the vicinity of Xq13.1 and is approximately 7 kb in length. This allele, which encodes…