3billion
back to listBack to List

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.
View More Disease Info
Disease NameOMIM IDInheritance
Speech-language disorder-1
602081AD

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results