Gene: SLC25A38 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54977
Gene Symbol: SLC25A38
SLC25A38 		0.340 GeneticVariation disease BEFREE Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia. 27038157 2016
Entrez Id: 54977
Gene Symbol: SLC25A38
SLC25A38 		0.340 GeneticVariation disease BEFREE Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia. 21393332 2011
Entrez Id: 54977
Gene Symbol: SLC25A38
SLC25A38 		0.340 GeneticVariation disease BEFREE Sideroblastic anemia due to SLC25A38 gene mutations, which is a mitochondrial transporter, is the next most common inherited sideroblastic anemia. 20848343 2010
Entrez Id: 54977
Gene Symbol: SLC25A38
SLC25A38 		0.340 Biomarker disease CTD_human Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. 19412178 2009
Entrez Id: 54977
Gene Symbol: SLC25A38
SLC25A38 		0.340 Biomarker disease BEFREE As recently occurred with the discovery of the SLC25A38-related sideroblastic anemia, the identification of the genes responsible for as yet uncharacterized forms will provide further insights into mitochondrial iron metabolism of erythroid cells and the pathophysiology of sideroblastic anemia. 19786205 2009