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 forkhead box protein P1, plays a role in the negative regulation of transcription. Mutation of the gene is associated with mental retardation with language impairment and autistic features. A translocation t(9;3)(p13;p14.1) of this gene with the PAX5 gene is associated with acute lymphoblastic leukemia. (NCI Thesaurus)

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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…

FOXO4 Gene

This gene plays a role in smooth muscle cell differentiation, cellular growth, cell cycle regulation and tumor suppression.

FOXO3 wt Allele

Human FOXO3 wild-type allele is located in the vicinity of 6q21 and is approximately 121 kb in length. This allele, which encodes…