Ornithine translocase
Ornithine translocase is responsible for transporting ornithine from the cytosol into the mitochondria in the urea cycle.
Pathology
A disorder is associated with ornithine translocase deficiency, and a form of hyperammonemia.
See also
External links
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By group |
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SLC1–10 |
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| SLC11–20 |
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- proton coupled metal ion transporter
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- human Na+-sulfate/carboxylate cotransporter
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- proton oligopeptide cotransporter
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- monocarboxylate transporter
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| SLC21–30 |
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- Na+-dependent ascorbic acid transporter
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- multifunctional anion exchanger
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(28): |
- Na+-coupled nucleoside transport (SLC28A1
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(29): |
- facilitative nucleoside transporter
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| SLC31–40 |
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- type II Na+-phosphate cotransporter
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(35): |
- nucleoside-sugar transporter
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- SLC35E1
- SLC35E2
- SLC35E3
- SLC35E4
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(36): |
- proton-coupled amino-acid transporter
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- sugar-phosphate/phosphate exchanger
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- System A & N, sodium-coupled neutral amino-acid transporter
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- basolateral iron transporter
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| SLC41–48 |
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- Na+-independent, system-L like amino-acid transporter
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- Putative sugar transporter
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see also solute carrier disorders |
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Main cycle | |
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Regulatory/transport | |
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