Gene: CUBN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8029
Gene Symbol: CUBN
CUBN 		0.110 GeneticVariation disease BEFREE Cubulin mutations cause a hereditary form of megaloblastic anemia secondary to vitamin B(12) deficiency, and proteinuria occurs in 50% of cases since cubilin is coreceptor for both the intestinal vitamin B(12)-intrinsic factor complex and the tubular reabsorption of protein in the proximal tubule. 21903995 2011
Entrez Id: 8029
Gene Symbol: CUBN
CUBN 		0.110 Biomarker disease HPO