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 Homo sapiens.

Ontology Information
PRO ID	PR:Q96BI1 Show OBO stanza / GPI
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

Related Cross References
DB identifiers	Reactome:R-HSA-561110, UniProtKB:Q96BI1

Interactive Sequence View Select/align proteoforms across species

Protein Forms Display Category: All All organism-gene
PRO ID & Category Annotation Complex Name Short Label Definition & Comment

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