Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54888
Gene Symbol: NSUN2
NSUN2
0.700 GeneticVariation disease UNIPROT Mutations in NSUN2 cause autosomal-recessive intellectual disability. 22541559 2012
Entrez Id: 54888
Gene Symbol: NSUN2
NSUN2
0.700 GeneticVariation disease UNIPROT Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability. 22541562 2012
Entrez Id: 54888
Gene Symbol: NSUN2
NSUN2
0.700 Biomarker disease GENOMICS_ENGLAND Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots. 21063731 2011
Entrez Id: 54888
Gene Symbol: NSUN2
NSUN2
0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 54888
Gene Symbol: NSUN2
NSUN2
0.700 Biomarker disease CTD_human
Entrez Id: 54888
Gene Symbol: NSUN2
NSUN2
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
Entrez Id: 255167
Gene Symbol: LINC01018
LINC01018
0.100 CausalMutation disease CLINVAR
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.100 GeneticVariation disease CLINVAR