Gene: FOXP2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2 		0.420 AlteredExpression disease BEFREE FOXP2 is a brain-expressed transcription factor implicated in a rare disorder involving speech apraxia and language impairments. 30104377 2018
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2 		0.420 Biomarker disease CTD_human Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. 27120335 2016
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2 		0.420 Biomarker disease BEFREE Notably, the patients were not able to laugh, cough, or sneeze spontaneously, replicating findings reported for two other FOXP2 cases and a potential diagnostic sign of nonsyndromic apraxia of speech. 22106036 2012
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2 		0.420 Biomarker disease CTD_human Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. 17033973 2006
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2 		0.420 Biomarker disease HPO