FOXP2 - Gene browser

FOXP2

forkhead box P2

HCNC Approved Symbol: FOXP2 (HGNC:13875)
Genomic Coordinates: 7:114,086,327 - 114,693,765 (7q31.1)
Synonyms: CAGH44, TNRC10, SPCH1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the FOXP2 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results