Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.610 GeneticVariation disease BEFREE Nephronophthisis-19 (NPHP19) due to truncating mutations in the DCDC2 gene has only been described previously in two patients. 31821705 2020
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.610 Biomarker disease GENOMICS_ENGLAND Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis. 27469900 2016
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.610 Biomarker disease GENOMICS_ENGLAND DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling. 25557784 2015
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.610 Biomarker disease GENOMICS_ENGLAND Exploring the transcriptome of ciliated cells using in silico dissection of human tissues. 22558177 2012
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.610 GeneticVariation disease CLINVAR
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.610 Biomarker disease CTD_human
Entrez Id: 51473
Gene Symbol: DCDC2
DCDC2 		0.610 CausalMutation disease CLINVAR
Entrez Id: 353219
Gene Symbol: KAAG1
KAAG1 		0.100 CausalMutation disease CLINVAR