SLC25A16: Difference between revisions

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


== References ==
== References ==
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[[Category:Human genes]]
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[[Category:Human proteins]]




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Latest revision as of 02:05, 25 September 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 is a protein in humans that is encoded by the SLC25A16 gene. [1]

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].

References

  1. ↑ "Entrez Gene: Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16". Retrieved 2012-11-27.

Further reading


Retrieved from "https://www.wikidoc.org/index.php?title=SLC25A16&oldid=1527404"