SLC25A16

Last updated
SLC25A16
Identifiers
Aliases SLC25A16 , D10S105E, GDA, GDC, HGT.1, ML7, hML7, solute carrier family 25 member 16
External IDs OMIM: 139080 MGI: 1920382 HomoloGene: 21858 GeneCards: SLC25A16
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_175194

RefSeq (protein)

NP_780403

Location (UCSC) Chr 10: 68.48 – 68.53 Mb Chr 10: 62.76 – 62.78 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 is a protein in humans that is encoded by the SLC25A16 gene. [5]

This gene encodes a protein that contains three tandemly repeated mitochondrial carrier protein domains. The encoded protein is localized in the inner membrane and facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. This gene has a possible role in Graves' disease. [provided by RefSeq, Jul 2008].

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Sodium/hydrogen exchanger 10, also known as solute carrier family 9 member 10, is a protein that in humans is encoded by the SLC9A10 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.

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Solute carrier family 8, member B1 is a protein that in humans is encoded by the SLC8B1 gene.

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<span class="mw-page-title-main">SLC22A24</span>

Solute carrier family 22 member 24 is a protein that in humans is encoded by the SLC22A24 gene.

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Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene.

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Solute carrier family 25 member 22 is a protein that in humans is encoded by the SLC25A22 gene. This gene encodes a mitochondrial glutamate carrier. Mutations in this gene are associated with early infantile epileptic encephalopathy. Expression of this gene is increased in colorectal tumor cells.

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<span class="mw-page-title-main">SLC25A46</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 25 member 46 is a protein that in humans is encoded by the SLC25A46 gene. This protein is a member of the SLC25 mitochondrial solute carrier family. It is a transmembrane protein located in the mitochondrial outer membrane involved in lipid transfer from the endoplasmic reticulum (ER) to mitochondria. Mutations in this gene result in neuropathy and optic atrophy.

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References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000122912 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000071253 - 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.
  5. "Entrez Gene: Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16" . Retrieved 2012-11-27.

Further reading