Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55180
Gene Symbol: LINS1
LINS1 		0.700 Biomarker disease GENOMICS_ENGLAND Worster-Drought Syndrome Associated With LINS Mutations. 30090841 2018
Entrez Id: 55180
Gene Symbol: LINS1
LINS1 		0.700 GeneticVariation disease UNIPROT Novel LINS1 missense mutation in a family with non-syndromic intellectual disability. 28181389 2017
Entrez Id: 55180
Gene Symbol: LINS1
LINS1 		0.700 GeneticVariation disease UNIPROT LINS, a modulator of the WNT signaling pathway, is involved in human cognition. 23773660 2013
Entrez Id: 55180
Gene Symbol: LINS1
LINS1 		0.700 GeneticVariation disease UNIPROT Deep sequencing reveals 50 novel genes for recessive cognitive disorders. 21937992 2011
Entrez Id: 55180
Gene Symbol: LINS1
LINS1 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 55180
Gene Symbol: LINS1
LINS1 		0.700 Biomarker disease CTD_human
Entrez Id: 55180
Gene Symbol: LINS1
LINS1 		0.700 CausalMutation disease CLINVAR
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