SLC40A1, solute carrier family 40 member 1, 30061

N. diseases: 101; N. variants: 31
Disease: Intravascular hemolysis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		0.310 GeneticVariation disease BEFREE Copper therapy reduces intravascular hemolysis and derepresses ferroportin in mice with mosaic mutation (Atp7a<sup>mo-ms</sup>): An implication for copper-mediated regulation of the Slc40a1 gene expression. 28219768 2017
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		0.310 Biomarker disease CTD_human Haemolysis and perturbations in the systemic iron metabolism of suckling, copper-deficient mosaic mutant mice - an animal model of Menkes disease. 25247420 2014