Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7991
Gene Symbol: TUSC3
TUSC3 		0.600 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 7991
Gene Symbol: TUSC3
TUSC3 		0.600 Biomarker disease GENOMICS_ENGLAND Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. 27148795 2016
Entrez Id: 7991
Gene Symbol: TUSC3
TUSC3 		0.600 Biomarker disease GENOMICS_ENGLAND A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian family. 21739581 2011
Entrez Id: 7991
Gene Symbol: TUSC3
TUSC3 		0.600 CausalMutation disease CLINVAR
Entrez Id: 7991
Gene Symbol: TUSC3
TUSC3 		0.600 Biomarker disease CTD_human
Entrez Id: 51185
Gene Symbol: CRBN
CRBN 		0.200 Biomarker disease MGD Rescue of Learning and Memory Deficits in the Human Nonsyndromic Intellectual Disability Cereblon Knock-Out Mouse Model by Targeting the AMP-Activated Protein Kinase-mTORC1 Translational Pathway. 29459374 2018
Entrez Id: 51185
Gene Symbol: CRBN
CRBN 		0.200 Biomarker disease MGD Behavioral characterization of cereblon forebrain-specific conditional null mice: a model for human non-syndromic intellectual disability. 21995942 2012