SLC47A1
SLC47A1 encodes a protein of unknown function. Lactic Acidosis and Smith-Magenis Syndrome are two conditions linked to SLC47A1. Transport of inorganic cations/anions, amino acids/oligopeptides, and atenolol route, pharmacokinetics are among its linked processes. Antiporter activity and monovalent cation:proton antiporter activity are two Gene Ontology (GO) annotations connected to this gene.
| Full Name | Solute carrier family 47 member 1 |
| Gene ID | Human: 55244 Mouse: 67473 Rat: 360539 Monkey: 703544 |
| UniProt ID | Human: Q96FL8 Mouse: Q8K0H1 Rat: Q5I0E9 Monkey: F7HN24 |
| Alternative Names | MATE1; multidrug and toxin extrusion protein 1; MATE-1; hMATE-1; multidrug and toxin extrusion 1; solute carrier family 47 (multidrug and toxin extrusion), member 1; SLC47A1; Solute carrier family 47 member 1 |
Product List
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mProX™ Human SLC47A1 Stable Cell Line
[CAT#: S01YF-1123-KX122]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: SLC47A1 Target Family: SLC Transporter Target Protein Species: Human Host Cell Type: CHO-K1; HEK293
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