Homo sapiens Gene: SLC22A18
Summary
InnateDB Gene IDBG-23534.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC22A18
Gene Name solute carrier family 22, member 18
Synonyms BWR1A; BWSCR1A; HET; IMPT1; ITM; ORCTL2; p45-BWR1A; SLC22A1L; TSSC5
Species Homo sapiens
Ensembl Gene ENSG00000110628
Encoded Proteins
solute carrier family 22, member 18
solute carrier family 22, member 18
solute carrier family 22, member 18
solute carrier family 22, member 18
solute carrier family 22, member 18
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Two alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Oct 2010]
This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms\' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Two alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Oct 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:2899721-2925246
Strand Forward strand
Band p15.4
Transcripts
ENST00000347936 ENSP00000307859
ENST00000312221 ENSP00000311139
ENST00000380574 ENSP00000369948
ENST00000449793 ENSP00000392072
ENST00000441077
ENST00000449603
ENST00000485423 ENSP00000433019
ENST00000492567
ENST00000498244
ENST00000467719
ENST00000463571
ENST00000498209
ENST00000495518
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
Experimentally validated
Total 6 [view]
Protein-Protein 4 [view]
Protein-DNA 2 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005215 transporter activity
GO:0015238 drug transmembrane transporter activity
GO:0015293 symporter activity
GO:0031625 ubiquitin protein ligase binding
Biological Process
GO:0006855 drug transmembrane transport
GO:0007588 excretion
GO:0015695 organic cation transport
GO:0015893 drug transport
GO:0055085 transmembrane transport
Cellular Component
GO:0005635 nuclear envelope
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016324 apical plasma membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Organic cation transport pathway
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway
Transmembrane transport of small molecules pathway
Organic cation/anion/zwitterion transport pathway
SLC-mediated transmembrane transport pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.50868 Hs.690839
RefSeq NM_002555 NM_183233 XM_005252952 XM_006718243
HUGO
OMIM
CCDS CCDS7740
HPRD 04024
IMGT
EMBL
GenPept
RNA Seq Atlas