Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 Biomarker 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

Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 Biomarker CTD_human Identifying autism loci and genes by tracing recent shared ancestry. 18621663

2008

Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 Biomarker CTD_human A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha. 18057082

2008

Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 Biomarker CTD_human Mapping autism risk loci using genetic linkage and chromosomal rearrangements. 17322880

2007