Homo sapiens Gene: SLC25A38
Summary
InnateDB Gene IDBG-26767.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC25A38
Gene Name solute carrier family 25, member 38
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000144659
Encoded Proteins
solute carrier family 25, member 38
solute carrier family 25, member 38
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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.[provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 3:39383348-39397351
Strand Forward strand
Band p22.1
Transcripts
ENST00000273158 ENSP00000273158
ENST00000431510 ENSP00000394244
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0006783 heme biosynthetic process
GO:0006810 transport
GO:0030218 erythrocyte differentiation
Cellular Component
GO:0005743 mitochondrial inner membrane
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.369615 Hs.606636
RefSeq NM_017875
HUGO
OMIM
CCDS CCDS2685
HPRD 07925
IMGT
EMBL
GenPept
RNA Seq Atlas