solute carrier family 47 (multidrug and toxin extrusion), member 1
Symbol
SLC47A1
(may also be known as: None)
Organism
Human
Description
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]
Orthologs
| Symbol | Species | |
|---|---|---|
| uncharacterized_F1RD | Danio rerio | |
| Slc47a1 | Mus musculus | |
| Slc47a1 | Rattus norvegicus |
Links to external resources
Changes associated with this gene
| Identifier | Name | Type | Tissues | Organism | Gene | Data | Actions |
|---|---|---|---|---|---|---|---|
| DAA2900 | Gene expression of SLC47A1 decreases with age | Molecular | adipose tissue | Human | SLC47A1 | — | |
| DAA3932 | Gene expression of SLC47A1 increases with age | Molecular | skin | Human | SLC47A1 | — |
GO Terms
| GO ID | GO Term | GO Category | |
|---|---|---|---|
| GO:0015695 | organic cation transport | biological_process | |
| GO:0055085 | transmembrane transport | biological_process | |
| GO:0005624 | membrane fraction | cellular_component | |
| GO:0005886 | plasma membrane | cellular_component | |
| GO:0016020 | membrane | cellular_component | |
| GO:0016021 | integral to membrane | cellular_component | |
| GO:0005451 | monovalent cation:hydrogen antiporter activity | molecular_function | |
| GO:0015238 | drug transmembrane transporter activity | molecular_function | |
| GO:0015297 | antiporter activity | molecular_function | |