Version 5.4
Mus musculus Protein: Slc22a15
Summary
InnateDB Protein IDBP-267747.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Slc22a15
Protein Name solute carrier family 22 (organic anion/cation transporter), member 15
Synonyms
Species Mus musculus
Ensembl Protein ENSMUSP00000102541
InnateDB Gene IDBG-180049 (Slc22a15)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0022857 transmembrane transporter activity
Biological Process
GO:0006811 ion transport
GO:0008150 biological_process
GO:0055085 transmembrane transport
Cellular Component
GO:0005575 cellular_component
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID MGI:3607704
InterPro IPR005828 General substrate transporter
IPR011701 Major facilitator superfamily
IPR016196 Major facilitator superfamily domain, general substrate transporter
IPR020846 Major facilitator superfamily domain
PFAM PF00083
PF07690
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q504N2
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 242126
UniGene Mm.90204
RefSeq NP_001034460
MGI ID
MGI Symbol Slc22a15
OMIM
CCDS CCDS51022
HPRD
IMGT
EMBL AC165165 AK029695 BC152347
GenPept AAI52348 BAC26569

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca