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SLC25A38


Official Full Name
solute carrier family 25 member 38
Organism
Homo sapiens
Gene ID
54977
Background
This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia (anemia, sideroblastic, 2, pyridoxine-refractory). A related pseudogene is found on chromosome 1. [provided by RefSeq, Aug 2017]
Synonyms
SIDBA2

Cat.No. Product Name Price
SHH409756 shRNA set against Mouse SLC25A38 (NM_144793.1) Inquiry
SHH409760 shRNA set against Rat SLC25A38 (NM_001030032.1) Inquiry
SHL003334 shRNA set against Mouse Slc25a38(NM_144793.1) Inquiry
SHL003346 shRNA set against Human SLC25A38(NM_017875.2) Inquiry
Cat.No. Product Name Price
CDFR004156 Rat Slc25a38 cDNA Clone(NM_001030032.1) Inquiry
MiUTR1H-09487 SLC25A38 miRNA 3'UTR clone Inquiry
MiUTR1M-10815 SLC25A38 miRNA 3'UTR clone Inquiry
MiUTR1R-06820 SLC25A38 miRNA 3'UTR clone Inquiry
CDCB191345 Rabbit SLC25A38 ORF clone (XM_008260273.1) Inquiry
CDCH081582 Mouse Slc25a38 ORF clone (NM_144793.1) Inquiry
CDCR371185 Rat Slc25a38 ORF Clone(NM_001030032.1) Inquiry
CDCS414538 Human SLC25A38 ORF Clone (BC013194) Inquiry
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