Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26115
Gene Symbol: TANC2
TANC2 		0.510 Biomarker group GENOMICS_ENGLAND Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. 31616000 2019
Entrez Id: 26115
Gene Symbol: TANC2
TANC2 		0.510 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.410 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 6792
Gene Symbol: CDKL5
CDKL5 		0.400 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 6812
Gene Symbol: STXBP1
STXBP1 		0.370 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 6812
Gene Symbol: STXBP1
STXBP1 		0.370 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 1106
Gene Symbol: CHD2
CHD2 		0.360 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A 		0.360 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A 		0.360 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 2290
Gene Symbol: FOXG1
FOXG1 		0.350 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 5728
Gene Symbol: PTEN
PTEN 		0.350 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 6925
Gene Symbol: TCF4
TCF4 		0.350 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.350 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.340 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C 		0.340 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B 		0.340 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 23126
Gene Symbol: POGZ
POGZ 		0.340 Biomarker group CTD_human Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889 2017
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A 		0.330 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 1654
Gene Symbol: DDX3X
DDX3X 		0.330 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.330 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1 		0.330 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 1917
Gene Symbol: EEF1A2
EEF1A2 		0.330 Biomarker group CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 22907
Gene Symbol: DHX30
DHX30 		0.330 Biomarker group GENOMICS_ENGLAND Thus, our findings highlight the prominent role of translation control in development and function of the central nervous system and also provide molecular insight into how DHX30 dysfunction might cause a neurodevelopmental disorder. 29100085 2017