SLC25A38
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Official Full Name
solute carrier family 25, member 38 -
Overview
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. -
Synonyms
SLC25A38;solute carrier family 25, member 38;solute carrier family 25 member 38;FLJ20551;FLJ22703
Recombinant Proteins
- Human
- Mouse
- Rat
- Mus musculus
- Xenopus tropicalis (Western clawed frog) (Silurana tropicalis)
- Xenopus laevis
- Bovine
- Sheep
- E.coli
- Mammalian Cells
- HEK293
- GST
- His
- Non
- His&Fc&Avi
Involved Pathway
SLC25A38 involved in several pathways and played different roles in them. We selected most pathways SLC25A38 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with SLC25A38 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|
Protein Function
SLC25A38 has several biochemical functions, for example, transporter activity. Some of the functions are cooperated with other proteins, some of the functions could acted by SLC25A38 itself. We selected most functions SLC25A38 had, and list some proteins which have the same functions with SLC25A38. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| transporter activity | SLC5A11,SLC12A3,GOSR2,FABP7B,RLBP1,SYPB,CPNE6,SEC22A,SLC13A5,ATP5D |
Interacting Protein
SLC25A38 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with SLC25A38 here. Most of them are supplied by our site. Hope this information will be useful for your research of SLC25A38.
yjfC;EMG1;ZSCAN16;NOL12
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