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PRO ID
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| PRO name | uncharacterized protein SLC67A1-AS (human) |
| Synonyms | | PRO-Short-label: | EXACT: | hSLC22A18AS | | Gene-based: | RELATED: | BWR1B | BWSCR1B | ORCTL2S | SLC22A18AS | SLC22A1LS | SLC67A1-AS | | Other: | EXACT: | Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein (human) | organic cation transporter-like protein 2 antisense protein (human) | p27-Beckwith-Wiedemann region 1 B (human) | p27-BWR1B (human) | SLC67A1 antisense RNA (human) | solute carrier family 22 member 1-like antisense protein (human) | solute carrier family 22 member 18 antisense protein (human) |
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| Definition | "An uncharacterized protein SLC67A1-AS that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q8N1D0] |
| PRO Category | organism-gene |
| Parent | PR:000014987 uncharacterized protein SLC67A1-AS
PR:000029067 Homo sapiens protein
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| Gene Template | HGNC:10965 SLC22A18AS (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 |
0 | | | |
Term Hierarchy
Visualization |
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