Gene: FOXP1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.350 GeneticVariation group BEFREE Haploinsufficiency of the forkhead-box protein P1 (<i>FOXP1</i>) gene leads to a neurodevelopmental disorder termed FOXP1 syndrome. 29090079 2017
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.350 GeneticVariation group BEFREE Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders. 28741757 2017
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.350 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.350 GeneticVariation group BEFREE Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. 26647308 2016
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.350 Biomarker group BEFREE Interestingly, three of these genes, FOXP1, SF3B1 and DLG2, have previously been implicated in neurodevelopmental disorders. 26460480 2015
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.350 Biomarker group BEFREE Mutations in the transcription factor Forkhead box p1 (FOXP1) are causative for neurodevelopmental disorders such as autism. 26494785 2015