Mitochondrial glycine transporter: Difference between revisions
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{{Infobox gene}} |
Importing Wikidata short description: Protein-coding gene in the species Homo sapiens (shortdescs-in-category) |
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{{Short description|Protein-coding gene in the species Homo sapiens}} |
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{{Infobox gene}} |
{{Infobox gene}} |
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'''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]]. |
'''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]]. |
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{{Membrane transport proteins}} |
{{Membrane transport proteins}} |
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[[Category:Solute carrier family]] |
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{{gene-3-stub}} |
{{gene-3-stub}} |
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Latest revision as of 22:14, 3 March 2023
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| Aliases | SLC25A38, SIDBA2, solute carrier family 25 member 38 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 610819; MGI: 2384782; HomoloGene: 5553; GeneCards: SLC25A38; OMA:SLC25A38 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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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]
- ^ a b c GRCh38: Ensembl release 89: ENSG00000144659 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032519 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
 | This article on a gene on human chromosome 3 is a stub. You can help Wikipedia by expanding it. |