|
PRO ID
 |
|
| PRO name | solute carrier family 67 member A1 (human) |
| Synonyms | | PRO-Short-label: | EXACT: | hSLC67A1 | | Gene-based: | RELATED: | BWR1A | BWSCR1A | HET | IMPT1 | ITM | ORCTL2 | SLC22A18 | SLC22A1L | SLC67A1 | TSSC5 | | Other: | EXACT: | Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene A protein (human) | efflux transporter-like protein (human) | imprinted multi-membrane-spanning polyspecific transporter-related protein 1 (human) | ORCTL-2 (human) | organic cation transporter-like protein 2 (human) | p45-Beckwith-Wiedemann region 1 A (human) | p45-BWR1A (human) | solute carrier family 22 member 1-like (human) | solute carrier family 22 member 18 (human) | tumor-suppressing STF cDNA 5 protein (human) | tumor-suppressing subchromosomal transferable fragment candidate gene 5 protein (human) |
|
| Definition | "A solute carrier family 67 member A1 that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q96BI1] |
| PRO Category | organism-gene |
| Parent | PR:000014986 solute carrier family 67 member A1
PR:000029067 Homo sapiens protein
|
| Gene Template | HGNC:10964 SLC67A1 (human) |
| Taxon | NCBITaxon:9606 Homo sapiens |
| Terms by PRO Category |
| Organism-Independent |
Organism-Specific |
| Category |
Number of Terms |
Category |
Number of Terms | | Gene | 0 |
Organism-Gene |
1 |
| Sequence | 0 |
Organism-Sequence |
2 | | Modification | 0 |
Organism-Modification |
1 | | | |
Term Hierarchy
Visualization |
|
