Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8239
Gene Symbol: USP9X
USP9X 		0.700 Biomarker disease GENOMICS_ENGLAND De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations. 26833328 2016
Entrez Id: 8239
Gene Symbol: USP9X
USP9X 		0.700 GeneticVariation disease UNIPROT Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth. 24607389 2014
Entrez Id: 8239
Gene Symbol: USP9X
USP9X 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth. 24607389 2014
Entrez Id: 8239
Gene Symbol: USP9X
USP9X 		0.700 Biomarker disease CTD_human
Entrez Id: 8239
Gene Symbol: USP9X
USP9X 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 8239
Gene Symbol: USP9X
USP9X 		0.700 CausalMutation disease CLINVAR
Entrez Id: 1741
Gene Symbol: DLG3
DLG3 		0.200 Biomarker disease MGD Altered thalamocortical development in the SAP102 knockout model of intellectual disability. 27466188 2016
Entrez Id: 2664
Gene Symbol: GDI1
GDI1 		0.200 Biomarker disease MGD Cognitive impairment in Gdi1-deficient mice is associated with altered synaptic vesicle pools and short-term synaptic plasticity, and can be corrected by appropriate learning training. 18829665 2009