Gene: RAD21 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5885
Gene Symbol: RAD21
RAD21 		0.700 GeneticVariation disease BEFREE Mutations in five genes, encoding subunits of the cohesin complex (SMC1A, SMC3, RAD21) and its regulators (NIPBL, HDAC8), are responsible for ∼ 70% of CdLS cases. 23683030 2014
Entrez Id: 5885
Gene Symbol: RAD21
RAD21 		0.700 GeneticVariation disease BEFREE Mutations in genes encoding either regulators (NIPBL, HDAC8) or subunits (SMC1A, SMC3, RAD21) of the cohesin complex, are altogether found in approximately 65% of CdLS patients. 23313159 2013
Entrez Id: 5885
Gene Symbol: RAD21
RAD21 		0.700 Biomarker disease CLINGEN RAD21 mutations cause a human cohesinopathy. 22633399 2012
Entrez Id: 5885
Gene Symbol: RAD21
RAD21 		0.700 GermlineCausalMutation disease ORPHANET RAD21 mutations cause a human cohesinopathy. 22633399 2012
Entrez Id: 5885
Gene Symbol: RAD21
RAD21 		0.700 Biomarker disease CLINGEN Cohesin-dependent regulation of Runx genes. 17567667 2007
Entrez Id: 5885
Gene Symbol: RAD21
RAD21 		0.700 Biomarker disease CTD_human