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QuickView for SLC25A16;jsessionid=0796CDFD958B8921E0EEEEB4C2721324 (gene)


Gene Symbol:
SLC25A16 Homo sapiens Homo sapiens
Full name:
solute carrier family 25 member 16
Synonyms:
D10S105E, GDA, GDC, HGT.1, ML7, hML7, graves disease carrier protein, mitochondrial solute carrier protein homolog, solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16
Genomic Location:
Chr 10: 69912103-69957590
Description:
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.
Orthologs:
Mus musculus Rattus norvegicus Saccharomyces cerevisiae Schizosaccharomyces pombe Bos taurus Danio rerio Gallus gallus Canis lupus familiaris Pan troglodytes
External Links:
Entrez Gene
Transcription Factor
Binding Sites:
miRNA binding sites
(Source: TargetScan):
Cytogenetic Map:
chr 10
10q21.3