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Protein Ontology Report - hSLC22A18

PR:Q96BI1 - http://purl.obolibrary.org/obo/PR_Q96BI1
This page represents a class of proteins encompassing all the protein products of the SLC22A18 gene in human.
Ontology Information
PRO ID PR:Q96BI1 Show OBO stanza
PRO name solute carrier family 22 member 18 (human)
Synonyms
PRO-short-label: EXACT: hSLC22A18
Gene-based: RELATED: BWR1A | BWSCR1A | HET | IMPT1 | ITM | ORCTL2 | SLC22A18 | SLC22A1L | TSSC5
Other: EXACT: Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene A protein (human) | ORCTL-2 (human) | efflux transporter-like protein (human) | imprinted multi-membrane-spanning polyspecific transporter-related protein 1 (human) | organic cation transporter-like protein 2 (human) | p45-BWR1A (human) | p45-Beckwith-Wiedemann region 1 A (human) | solute carrier family 22 member 1-like (human) | tumor-suppressing STF cDNA 5 protein (human) | tumor-suppressing subchromosomal transferable fragment candidate gene 5 protein (human)
Definition A solute carrier family 22 member 18 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q96BI1]
PRO Category organism-gene
Parent PR:000014986 solute carrier family 22 member 18
Gene Template HGNC:10964 SLC22A18
Taxon NCBITaxon:9606 Homo sapiens
Terms by PRO Category Retrieve All terms OBO Stanza / PAF
Organism-Specific
Category Number of Terms
organism-gene 1
organism-sequence 0
organism-modification 0
Term Hierarchy Visualization DAG     OLS     Cytoscape


Interactive Sequence View Select/align proteoforms across species

Protein Forms
PRO ID & Category Annotation Complex Name Short Label Definition & Comment

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