Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1718
Gene Symbol: DHCR24
DHCR24
0.300 Biomarker disease CTD_human Disrupted brain thyroid hormone homeostasis and altered thyroid hormone-dependent brain gene expression in autism spectrum disorders. 24781735 2014
Entrez Id: 1735
Gene Symbol: DIO3
DIO3
0.300 Biomarker disease CTD_human Disrupted brain thyroid hormone homeostasis and altered thyroid hormone-dependent brain gene expression in autism spectrum disorders. 24781735 2014
Entrez Id: 6567
Gene Symbol: SLC16A2
SLC16A2
0.300 Biomarker disease CTD_human Disrupted brain thyroid hormone homeostasis and altered thyroid hormone-dependent brain gene expression in autism spectrum disorders. 24781735 2014
Entrez Id: 23152
Gene Symbol: CIC
CIC
0.300 Biomarker disease CTD_human Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans. 28288114 2017
Entrez Id: 2020
Gene Symbol: EN2
EN2
0.590 Biomarker disease CTD_human Elevated 5-hydroxymethylcytosine in the Engrailed-2 (EN-2) promoter is associated with increased gene expression and decreased MeCP2 binding in autism cerebellum. 25290267 2014
Entrez Id: 1788
Gene Symbol: DNMT3A
DNMT3A
0.310 Biomarker disease CTD_human Elevated 5-hydroxymethylcytosine in the Engrailed-2 (EN-2) promoter is associated with increased gene expression and decreased MeCP2 binding in autism cerebellum. 25290267 2014
Entrez Id: 80312
Gene Symbol: TET1
TET1
0.310 Biomarker disease CTD_human Elevated 5-hydroxymethylcytosine in the Engrailed-2 (EN-2) promoter is associated with increased gene expression and decreased MeCP2 binding in autism cerebellum. 25290267 2014
Entrez Id: 1789
Gene Symbol: DNMT3B
DNMT3B
0.300 Biomarker disease CTD_human Elevated 5-hydroxymethylcytosine in the Engrailed-2 (EN-2) promoter is associated with increased gene expression and decreased MeCP2 binding in autism cerebellum. 25290267 2014
Entrez Id: 200424
Gene Symbol: TET3
TET3
0.300 Biomarker disease CTD_human Elevated 5-hydroxymethylcytosine in the Engrailed-2 (EN-2) promoter is associated with increased gene expression and decreased MeCP2 binding in autism cerebellum. 25290267 2014
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
0.700 Biomarker disease CTD_human Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. 21572417 2011
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
0.530 Biomarker disease CTD_human Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. 21572417 2011
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
0.380 Biomarker disease CTD_human Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. 21572417 2011
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1
0.370 Biomarker disease CTD_human Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. 21572417 2011
Entrez Id: 10319
Gene Symbol: LAMC3
LAMC3
0.300 Biomarker disease CTD_human Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. 21572417 2011
Entrez Id: 3690
Gene Symbol: ITGB3
ITGB3
0.370 Biomarker disease CTD_human Given the lack of previous data on the impact of integrin β3 on brain or behavioral phenotypes, we sought to compare mice with decreased or absent expression of the integrin β3 receptor subunit (Itgb3 +/- and -/-) with wildtype littermate controls in behavioral tasks relevant to ASD. 21254450 2011
Entrez Id: 25942
Gene Symbol: SIN3A
SIN3A
0.310 Biomarker disease CTD_human Here we identified dominant mutations in the gene encoding the transcriptional repressor and MeCP2 interactor switch-insensitive 3 family member A (SIN3A; chromosome 15q24.2) in individuals who, in addition to mild intellectual disability and ASD, share striking features, including facial dysmorphisms, microcephaly and short stature. 27399968 2016
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C
0.410 Biomarker disease CTD_human Here we present two additional patients with severe MR, autism spectrum disorder and epilepsy, carrying a very small deletion encompassing the MEF2C gene. 20412115 2010
Entrez Id: 4543
Gene Symbol: MTNR1A
MTNR1A
0.320 Biomarker disease CTD_human Here, we sequenced the melatonin receptor MTNR1A and MTNR1B, genes coding for MT1 and MT2 receptors, respectively, in a large panel of 941 individuals including 295 patients with ASD, 362 controls and 284 individuals from different ethnic backgrounds. 20657642 2010
Entrez Id: 4544
Gene Symbol: MTNR1B
MTNR1B
0.310 Biomarker disease CTD_human Here, we sequenced the melatonin receptor MTNR1A and MTNR1B, genes coding for MT1 and MT2 receptors, respectively, in a large panel of 941 individuals including 295 patients with ASD, 362 controls and 284 individuals from different ethnic backgrounds. 20657642 2010
Entrez Id: 57680
Gene Symbol: CHD8
CHD8
0.800 Biomarker disease CLINGEN Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-β-catenin signaling pathway. 22083958 2012
Entrez Id: 79742
Gene Symbol: DIPK2B
DIPK2B
0.310 Biomarker disease CTD_human Human genes c3orf58 or Deleted In Autism-1 (DIA1) and cXorf36 or Deleted in Autism-1 Related (DIA1R) are implicated in ASD and mental retardation. 21283809 2011
Entrez Id: 2053
Gene Symbol: EPHX2
EPHX2
0.300 Biomarker disease CTD_human Key role of soluble epoxide hydrolase in the neurodevelopmental disorders of offspring after maternal immune activation. 30890645 2019
Entrez Id: 57680
Gene Symbol: CHD8
CHD8
0.800 Biomarker disease CLINGEN Mutations in chromodomain helicase DNA-binding domain 8 (CHD8) have been identified in independent genotyping studies of autism spectrum disorder. 26789910 2016
Entrez Id: 95681
Gene Symbol: CEP41
CEP41
0.320 Biomarker disease CTD_human Mutations in the TSGA14 gene in families with autism spectrum disorders. 21438139 2011
Entrez Id: 85358
Gene Symbol: SHANK3
SHANK3
0.700 Biomarker disease CTD_human Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. 17173049 2007