Aliases for SLC25A16 Gene
External Ids for SLC25A16 Gene
Previous GeneCards Identifiers for SLC25A16 Gene
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]
GeneCards Summary for SLC25A16 Gene
SLC25A16 (Solute Carrier Family 25 Member 16) is a Protein Coding gene. Diseases associated with SLC25A16 include Isolated Nail Anomaly and Nonsyndromic Congenital Nail Disorder. Among its related pathways are Metabolism of water-soluble vitamins and cofactors and Metabolism. Gene Ontology (GO) annotations related to this gene include antiporter activity. An important paralog of this gene is SLC25A42.
UniProtKB/Swiss-Prot Summary for SLC25A16 Gene
Required for the accumulation of coenzyme A in the mitochondrial matrix.