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 		0.020 GeneticVariation disease BEFREE We found reduced mRNA and protein expression of FOXP2 in frontal cortex area 8 in Pick's disease, and frontotemporal lobar degeneration-tau linked to P301L mutation presenting with language impairment in comparison with age-matched controls and cases with parkinsonian variant progressive supranuclear palsy. 27497476 2016
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2 		0.020 GeneticVariation disease BEFREE No significant differences of the four FOXP2 polymorphisms in genotype distribution and allele frequency between FTLD and controls were observed. 20858950 2010