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Protein Ontology Report - hSLC22A18

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)
PRO-short-label: hSLC22A18
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)
Gene-based: BWR1A; BWSCR1A; HET; IMPT1; ITM; ORCTL2; SLC22A18; SLC22A1L; TSSC5
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
Terms by PRO Category Retrieve All terms OBO Stanza / PAF
Category Number of Terms
organism-gene 1
organism-sequence 0
organism-modification 0
Term Hierarchy Visualization DAG     OLS     Cytoscape

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