SLC25A16
Sign in to saveAlso known as D10S105E, GDA, GDC, HGT.1, ML7, hML7, solute carrier family 25 member 16
Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 is a protein in humans that is encoded by the SLC25A16 gene.
Gene data
SLC25A16- Name
- solute carrier family 25 member 16
- Type
- protein-coding
- Position
- 68,473,079–68,527,539 (−)
- Aliases
- D10S105E, GDA, GDC, HGT.1, ML7, hGP, hML7
- Ensembl
- ENSG00000122912
- RefSeq RNA
- NM_001324312.2, NM_001324313.2, NM_001324314.2, NM_001324315.1, NM_001324317.2
- RefSeq protein
- NP_001311241.1, NP_001311242.1, NP_001311243.1, NP_001311244.1, NP_001311246.1
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].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
solute carrier family 25 member 16
- Symbol
- SLC25A16
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 10:68,473,079-68,527,539
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- Further reading
Solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 is a protein in humans that is encoded by the 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].
Excerpted from Wikipedia’s “SLC25A16” article, available under the CC BY-SA 4.0 licence.