Synonyms:D10S105E, ENTREZ:8034, GDA, GDC, HGNC:10986, HGT.1, MIM:139080, ML7, NM_001324312, NM_001324313, NM_001324314, NM_001324315, NM_001324317, NM_152707, NP_001311241, NP_001311242, NP_001311243, NP_001311244, NP_001311246, NP_689920, NR_136737, SLC25A16, hML7, solute carrier family 25 member 16
Omim:OMIM:139080
Id:ENSG00000122912
Hgnc:HGNC:10986
Description:solute carrier family 25 member 16
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]