SLC25A16

SLC25A16
Identifiers
Aliases	SLC25A16, D10S105E, GDA, GDC, HGT.1, ML7, hML7, solute carrier family 25 member 16
External IDs	MGI: 1920382 HomoloGene: 21858 GeneCards: SLC25A16
Gene ontology Molecular function • structural constituent of ribosome • antiporter activity • secondary active transmembrane transporter activity Cellular component • integral component of membrane • mitochondrial inner membrane • membrane • mitochondrion Biological process • coenzyme biosynthetic process • translation • transmembrane transport • transport Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	8034	73132
Ensembl	ENSG00000122912	ENSMUSG00000071253
UniProt	P16260	Q8C0K5
RefSeq (mRNA)	NM_152707 NM_001324312 NM_001324313 NM_001324314 NM_001324315 NM_001324317	NM_175194
RefSeq (protein)	NP_689920.1	NP_780403.1
Location (UCSC)	Chr 10: 68.48 – 68.53 Mb	Chr 10: 62.92 – 62.95 Mb
PubMed search	[1]	[2]
Wikidata

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Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 is a protein in humans that is encoded by the SLC25A16 gene. ^[3]

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. "Human PubMed Reference:".
2. "Mouse PubMed Reference:".
3. "Entrez Gene: Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16". Retrieved 2012-11-27.

Further reading