Gene: NRXN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1 		0.600 GeneticVariation disease CLINVAR Fraternal twins with autism, severe cognitive deficit, and epilepsy: diagnostic role of chromosomal microarray analysis. 25149956 2014
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1 		0.600 Biomarker disease GENOMICS_ENGLAND Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions. 22617343 2012
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1 		0.600 GeneticVariation disease CLINVAR Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters. 21964664 2011
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1 		0.600 GeneticVariation disease CLINVAR CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila. 19896112 2009
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1 		0.600 Biomarker disease CTD_human
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1 		0.600 CausalMutation disease CLINVAR