SLC22A5: Difference between revisions
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* {{MeshName|SLC22A5+protein,+human}} |
* {{MeshName|SLC22A5+protein,+human}} |
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{{Membrane transport proteins}} |
{{Membrane transport proteins}} |
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[[Category:Transmembrane proteins]] |
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Revision as of 06:45, 14 December 2007
| solute carrier family 22 (organic cation transporter), member 5 | |||||||
|---|---|---|---|---|---|---|---|
| Identifiers | |||||||
| Symbol | SLC22A5 | ||||||
| Alt. symbols | CDSP | ||||||
| NCBI gene | 6584 | ||||||
| HGNC | 10969 | ||||||
| OMIM | 603377 | ||||||
| RefSeq | NM_003060 | ||||||
| UniProt | O76082 | ||||||
| Other data | |||||||
| Locus | Chr. 5 q31 | ||||||
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SLC22A5 is a membrane transport protein associated with primary carnitine deficiency.
External links
- SLC22A5+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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