Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1. 30385778

2018
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN Targeted Next-Generation Sequencing of Korean Patients With Developmental Delay and/or Intellectual Disability. 30631761

2018
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome. 29330474

2018
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN Foxp1 regulation of neonatal vocalizations via cortical development. 29138280

2017
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability? 28884888

2017
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN FOXP1-related intellectual disability syndrome: a recognisable entity. 28735298

2017
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene. 27657687

2017
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN 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
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment. 25853299

2015
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN Foxp1 regulates cortical radial migration and neuronal morphogenesis in developing cerebral cortex. 26010426

2015
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment. 25767709

2015
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN FoxP1 orchestration of ASD-relevant signaling pathways in the striatum. 26494785

2015
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech. 24083349

2013
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN FOXP1 mutations cause intellectual disability and a recognizable phenotype. 24214399

2013
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. 20950788

2010
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		0.500 Biomarker CLINGEN Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. 12687690

2003