Ornithine translocase is responsible for transporting ornithine from the cytosol into the mitochondria in the urea cycle. It is highly expressed in the liver and pancreas.
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 | |||||||
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Identifiers | |||||||
Symbol | SLC25A15 | ||||||
Alt. symbols | ORNT1, HHH | ||||||
NCBI gene | 10166 | ||||||
HGNC | 10985 | ||||||
OMIM | 603861 | ||||||
RefSeq | NM_014252 | ||||||
UniProt | Q9Y619 | ||||||
Other data | |||||||
Locus | Chr. 13 q14 | ||||||
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Pathology
editA disorder is associated with ornithine translocase deficiency, and a form of hyperammonemia.
See also
editExternal links
edit- ornithine+translocase at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- SLC25A15 human gene location in the UCSC Genome Browser.
- SLC25A15 human gene details in the UCSC Genome Browser.