NRXN1, neurexin 1, 9378

N. diseases: 20; N. variants: 26
Disease: Autistic Disorder ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.700 Biomarker disease CTD_human At a gene level, CAM genes associated in all three samples (NRXN1 and CNTNAP2), which were previously implicated in specific language disorder, autism and schizophrenia. 20157312 2011
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.700 Biomarker disease CTD_human Identifying autism loci and genes by tracing recent shared ancestry. 18621663 2008
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.700 Biomarker disease CTD_human A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha. 18057082 2008
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.700 Biomarker disease CTD_human Mapping autism risk loci using genetic linkage and chromosomal rearrangements. 17322880 2007
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.700 Biomarker disease GENOMICS_ENGLAND