Homo sapiens Protein: SLC22A18
Summary
InnateDB Protein IDBP-23538.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC22A18
Protein Name solute carrier family 22, member 18
Synonyms BWR1A; BWSCR1A; HET; IMPT1; ITM; ORCTL2; p45-BWR1A; SLC22A1L; TSSC5;
Species Homo sapiens
Ensembl Protein ENSP00000307859
InnateDB Gene IDBG-23534 (SLC22A18)
Protein Structure
UniProt Annotation
Function May act as a transporter of organic cations based on a proton efflux antiport mechanism. May play a role in the transport of chloroquine and quinidine-related compounds in kidney. {ECO:0000269PubMed:9744804}.
Subcellular Localization Apical cell membrane {ECO:0000305}; Multi- pass membrane protein {ECO:0000305}. Note=Localized at the apical membrane surface of renal proximal tubules. {ECO:0000269PubMed:9744804}.
Disease Associations Lung cancer (LNCR) [MIM:211980]: A common malignancy affecting tissues of the lung. The most common form of lung cancer is non-small cell lung cancer (NSCLC) that can be divided into 3 major histologic subtypes: squamous cell carcinoma, adenocarcinoma, and large cell lung cancer. NSCLC is often diagnosed at an advanced stage and has a poor prognosis. {ECO:0000269PubMed:9751628}. Note=The gene represented in this entry may be involved in disease pathogenesis.Rhabdomyosarcoma, embryonal, 1 (RMSE1) [MIM:268210]: A form of rhabdomyosarcoma, a highly malignant tumor of striated muscle derived from primitive mesenchymal cells and exhibiting differentiation along rhabdomyoblastic lines. Rhabdomyosarcoma is one of the most frequently occurring soft tissue sarcomas and the most common in children. It occurs in four forms: alveolar, pleomorphic, embryonal and botryoidal rhabdomyosarcomas. Note=The disease may be caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed at high levels in adult and fetal kidney and liver, and adult colon. Expressed in fetal renal proximal tubules (at protein level). Expressed at lower levels in heart, brain and lung. {ECO:0000269PubMed:9499412, ECO:0000269PubMed:9520460, ECO:0000269PubMed:9570947, ECO:0000269PubMed:9744804}.
Comments
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: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
Protein Structure and Domains
PDB ID
InterPro IPR001958 Tetracycline resistance protein, TetA/multidrug resistance protein MdtG
IPR011701 Major facilitator superfamily
IPR016196 Major facilitator superfamily domain, general substrate transporter
IPR020846 Major facilitator superfamily domain
PFAM PF07690
PRINTS PR01035
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q96BI1
PhosphoSite PhosphoSite-Q96BI1
TrEMBL Q69YM4
UniProt Splice Variant
Entrez Gene 5002
UniGene Hs.690839
RefSeq NP_899056
HUGO HGNC:10964
OMIM 602631
CCDS CCDS7740
HPRD 04024
IMGT
EMBL AB012083 AC013791 AF028738 AF030302 AF037064 AF059663 AF070479 AL832892 BC015571
GenPept AAB82727 AAC04787 AAC14725 AAC17492 AAC23505 AAH15571 BAA32779 CAH10416