Pub. Date : 1993
PMID : 22649802
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | DIAGNOSIS/TESTING: HHH syndrome is caused by mutation of SLC25A15, the gene that encodes ORNT1 (mitochondrial ornithine transporter 1), which is involved in the urea cycle and the ornithine degradation pathway. | Ornithine | solute carrier family 25 member 15 | Homo sapiens |
| 2 | DIAGNOSIS/TESTING: HHH syndrome is caused by mutation of SLC25A15, the gene that encodes ORNT1 (mitochondrial ornithine transporter 1), which is involved in the urea cycle and the ornithine degradation pathway. | Ornithine | solute carrier family 25 member 15 | Homo sapiens |