Homo sapiens Gene: SLC5A2
Summary
InnateDB Gene IDBG-28583.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC5A2
Gene Name solute carrier family 5 (sodium/glucose cotransporter), member 2
Synonyms SGLT2
Species Homo sapiens
Ensembl Gene ENSG00000140675
Encoded Proteins
solute carrier family 5 (sodium/glucose cotransporter), member 2
solute carrier family 5 (sodium/glucose cotransporter), member 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the sodium glucose cotransporter family which are sodium-dependent glucose transport proteins. The encoded protein is the major cotransporter involved in glucose reabsorption in the kidney. Mutations in this gene are associated with renal glucosuria. [provided by RefSeq, Sep 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:31483002-31490860
Strand Forward strand
Band p11.2
Transcripts
ENST00000330498 ENSP00000327943
ENST00000419665 ENSP00000410601
ENST00000565446
ENST00000562006
ENST00000567051
ENST00000568188
ENST00000568891
ENST00000564197
ENST00000569576 ENSP00000455143
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:0005215 transporter activity
GO:0005362 low-affinity glucose:sodium symporter activity
GO:0005515 protein binding
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0006810 transport
GO:0006814 sodium ion transport
GO:0015758 glucose transport
GO:0055085 transmembrane transport
Cellular Component
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Inositol transporters pathway
Na+-dependent glucose transporters pathway
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway
Hexose transport pathway
Transmembrane transport of small molecules pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Orphan transporters pathway
Metabolism pathway
SLC-mediated transmembrane transport pathway
Disease pathway
Glycogen storage diseases pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.663690 Hs.709195
RefSeq NM_003041 XM_006721073
HUGO
OMIM
CCDS CCDS10714
HPRD 08919
IMGT
EMBL
GenPept
RNA Seq Atlas