Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 10716
Gene Symbol: TBR1
TBR1
0.650 Biomarker disease CTD_human
Entrez Id: 50944
Gene Symbol: SHANK1
SHANK1
0.530 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 55217
Gene Symbol: TMLHE
TMLHE
0.460 Biomarker disease CTD_human
Entrez Id: 6638
Gene Symbol: SNRPN
SNRPN
0.410 Biomarker disease CTD_human
Entrez Id: 1977
Gene Symbol: EIF4E
EIF4E
0.320 Biomarker disease CTD_human
Entrez Id: 9379
Gene Symbol: NRXN2
NRXN2
0.320 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 36
Gene Symbol: ACADSB
ACADSB
0.300 Biomarker disease CTD_human 2-methylbutyryl-CoA dehydrogenase deficiency associated with autism and mental retardation: a case report. 17883863 2007
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
0.320 Biomarker disease CTD_human Autistic phenotype from MEF2C knockout cells. 19131610 2009
Entrez Id: 5080
Gene Symbol: PAX6
PAX6
0.530 Biomarker disease CTD_human Pax6 3' deletion results in aniridia, autism and mental retardation. 18322702 2008
Entrez Id: 9855
Gene Symbol: FARP2
FARP2
0.310 Biomarker disease CTD_human FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome. 19365831 2009
Entrez Id: 2332
Gene Symbol: FMR1
FMR1
0.500 Biomarker disease CTD_human FMR1 gene expansion, large deletion of Xp, and skewed X-inactivation in a girl with mental retardation and autism. 20425835 2010
Entrez Id: 349075
Gene Symbol: ZNF713
ZNF713
0.300 Biomarker disease GENOMICS_ENGLAND A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two families. 25196122 2014
Entrez Id: 1814
Gene Symbol: DRD3
DRD3
0.330 Biomarker disease CTD_human A common variant in DRD3 receptor is associated with autism spectrum disorder. 19058789 2009
Entrez Id: 26056
Gene Symbol: RAB11FIP5
RAB11FIP5
0.300 Biomarker disease CTD_human A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder. 18384058 2008
Entrez Id: 1812
Gene Symbol: DRD1
DRD1
0.320 Biomarker disease CTD_human A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families. 18205172 2008
Entrez Id: 6573
Gene Symbol: SLC19A1
SLC19A1
0.310 Biomarker disease CTD_human A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism. 20468076 2010
Entrez Id: 140733
Gene Symbol: MACROD2
MACROD2
0.430 Biomarker disease CTD_human A genome-wide scan for common alleles affecting risk for autism. 20663923 2010
Entrez Id: 9013
Gene Symbol: TAF1C
TAF1C
0.400 Biomarker disease CTD_human A genome-wide scan for common alleles affecting risk for autism. 20663923 2010
Entrez Id: 8128
Gene Symbol: ST8SIA2
ST8SIA2
0.330 Biomarker disease CTD_human A genome-wide scan for common alleles affecting risk for autism. 20663923 2010
Entrez Id: 23078
Gene Symbol: VWA8
VWA8
0.310 Biomarker disease CTD_human A genome-wide scan for common alleles affecting risk for autism. 20663923 2010
Entrez Id: 11281
Gene Symbol: POU6F2
POU6F2
0.300 Biomarker disease CTD_human A genome-wide scan for common alleles affecting risk for autism. 20663923 2010
Entrez Id: 200150
Gene Symbol: PLD5
PLD5
0.300 Biomarker disease CTD_human A genome-wide scan for common alleles affecting risk for autism. 20663923 2010
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
0.700 Biomarker disease CTD_human A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha. 18057082 2008
Entrez Id: 23394
Gene Symbol: ADNP
ADNP
0.500 Biomarker disease CTD_human A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. 24531329 2014