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 		0.120 GeneticVariation disease BEFREE FOXP1(R525X) is a de novo heterozygous mutation found in patients with autism and severe mental retardation. 30124790 2019
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.120 Biomarker disease BEFREE Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability. 29969624 2018
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.120 CausalMutation disease CLINVAR