Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 Biomarker disease GENOMICS_ENGLAND Genetic variations on SETD5 underlying autistic conditions. 29484850 2018
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 GeneticVariation disease UNIPROT SETD5 gene variant associated with mild intellectual disability - a case report. 28549204 2017
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 GeneticVariation disease UNIPROT SETD5 loss-of-function mutation as a likely cause of a familial syndromic intellectual disability with variable phenotypic expression. 27375234 2016
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 GeneticVariation disease UNIPROT Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome. 25138099 2015
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 GermlineCausalMutation disease ORPHANET De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability. 24680889 2014
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 Biomarker disease GENOMICS_ENGLAND De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability. 24680889 2014
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 GeneticVariation disease UNIPROT De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability. 24680889 2014
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 CausalMutation disease CLINVAR
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 55209
Gene Symbol: SETD5
SETD5 		0.700 Biomarker disease CTD_human