Ornithine translocase
Ornithine translocase is responsible for transporting ornithine from the cytosol into the mitochondria in the urea cycle.
| solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 | |
|---|---|
| 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 |
Pathology
A disorder is associated with ornithine translocase deficiency, and a form of hyperammonemia.
gollark: Now I just need to find the other ~5 million sandboxbreaking bugs!
gollark: Also, load is limited to taking `t` as that third mode arg, right?
gollark: Amazing!
gollark: Is there some horrible sandbox-breaking issue you didn't mention, then?
gollark: Is there some other horrible sandbox-breaking issue which this won't cover then?
See also
External links
- ornithine+translocase at the US 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.
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