Mus musculus Gene: Slc22a5
Summary
InnateDB Gene IDBG-172348.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Slc22a5
Gene Name solute carrier family 22 (organic cation transporter), member 5
Synonyms jvs; Lstpl; Octn2
Species Mus musculus
Ensembl Gene ENSMUSG00000018900
Encoded Proteins
solute carrier family 22 (organic cation transporter), member 5
solute carrier family 22 (organic cation transporter), member 5
solute carrier family 22 (organic cation transporter), member 5
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000197375:
Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:53864542-53891660
Strand Reverse strand
Band B1.3
Transcripts
ENSMUST00000019044 ENSMUSP00000019044
ENSMUST00000152084 ENSMUSP00000115474
ENSMUST00000136307 ENSMUSP00000118900
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005524 ATP binding
GO:0015075 ion transmembrane transporter activity
GO:0015226 carnitine transmembrane transporter activity
GO:0015293 symporter activity
GO:0015651 quaternary ammonium group transmembrane transporter activity
GO:0022857 transmembrane transporter activity
Biological Process
GO:0006814 sodium ion transport
GO:0007005 mitochondrion organization
GO:0007512 adult heart development
GO:0007626 locomotory behavior
GO:0009437 carnitine metabolic process
GO:0015697 quaternary ammonium group transport
GO:0015879 carnitine transport
GO:0034220 ion transmembrane transport
GO:0048608 reproductive structure development
GO:0055085 transmembrane transport
GO:1902603 carnitine transmembrane transport
Cellular Component
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016324 apical plasma membrane
GO:0031526 brush border membrane
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway
SLC-mediated transmembrane transport pathway
Transmembrane transport of small molecules pathway
Organic cation/anion/zwitterion transport pathway
Organic cation transport pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
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 F6TNN8
UniProt Splice Variant
Entrez Gene 20520
UniGene Mm.42253
RefSeq NM_011396
OMIM
CCDS CCDS24687
HPRD
IMGT
MGI ID MGI:1329012
MGI Symbol Slc22a5
EMBL AL596182
GenPept
RNA Seq Atlas 20520