SLC25A16

Solute carrier family 25 (mitochondrial carrier), member 16
Identifiers
Symbols	SLC25A16 ; D10S105E; GDA; GDC; HGT.1; ML7; hML7
External IDs	OMIM: 139080 HomoloGene: 21858 IUPHAR: 1071 GeneCards: SLC25A16 Gene
Gene ontology Molecular function • antiporter activity Cellular component • mitochondrial inner membrane • integral component of membrane Biological process • vitamin metabolic process • water-soluble vitamin metabolic process • transport • coenzyme biosynthetic process • pantothenate metabolic process • small molecule metabolic process • transmembrane transport Sources: Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	8034	73132
Ensembl	ENSG00000122912	ENSMUSG00000071253
UniProt	P16260	Q8C0K5
RefSeq (mRNA)	NM_152707	NM_175194
RefSeq (protein)	NP_689920	NP_780403
Location (UCSC)	Chr 10: 68.48 – 68.53 Mb	Chr 10: 62.92 – 62.95 Mb
PubMed search

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