Mitochondrial glycine transporter

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SLC25A38
Identifiers
AliasesSLC25A38, SIDBA2, solute carrier family 25 member 38
External IDsOMIM: 610819 MGI: 2384782 HomoloGene: 5553 GeneCards: SLC25A38
Gene location (Human)
Chromosome 3 (human)
Chr.Chromosome 3 (human)[1]
Chromosome 3 (human)
Genomic location for SLC25A38
Genomic location for SLC25A38
Band3p22.1Start39,383,370 bp[1]
End39,397,351 bp[1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_017875
NM_001354798

NM_144793

RefSeq (protein)

NP_060345
NP_001341727

NP_659042

Location (UCSC)Chr 3: 39.38 – 39.4 MbChr 9: 120.11 – 120.12 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Mitochondrial glycine transporter is a protein that in humans is encoded by the SLC25A38 gene. SLC25A38 is involved in mitochondrial handling of glycine and is needed for the first step in heme synthesis. Mutations in this gene can lead to an autosomal recessive form of sideroblastic anemia.

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000144659 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032519 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.