SLC11A2, solute carrier family 11 member 2, 4891

N. diseases: 99; N. variants: 13
Disease: Parkinsonian Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.210 Biomarker group RGD Up-regulation of divalent metal transporter 1 in 6-hydroxydopamine intoxication is IRE/IRP dependent. 20125122 2010
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.210 GeneticVariation group BEFREE A mutation in DMT1 that impairs iron transport protected rodents against parkinsonism-inducing neurotoxins MPTP and 6-hydroxydopamine (6-OHDA). 20082992 2009
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.210 Biomarker group RGD In addition, we report that a mutation in DMT1 that impairs iron transport protects rodents against parkinsonism-inducing neurotoxins MPTP and 6-hydroxydopamine. 19011085 2008