Homo sapiens Gene: SLC28A2
Summary
InnateDB Gene IDBG-10318.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC28A2
Gene Name solute carrier family 28 (sodium-coupled nucleoside transporter), member 2
Synonyms CNT2; HCNT2; HsT17153; SPNT1
Species Homo sapiens
Ensembl Gene ENSG00000137860
Encoded Proteins
solute carrier family 28 (sodium-coupled nucleoside transporter), member 2
solute carrier family 28 (sodium-coupled nucleoside transporter), member 2
solute carrier family 28 (sodium-coupled nucleoside transporter), member 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 15:45252230-45277845
Strand Forward strand
Band q21.1
Transcripts
ENST00000347644 ENSP00000315006
ENST00000560438 ENSP00000454074
ENST00000559924 ENSP00000454046
ENST00000560767
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:0001882 nucleoside binding
GO:0005415 nucleoside:sodium symporter activity
GO:0015211 purine nucleoside transmembrane transporter activity
Biological Process
GO:0006139 nucleobase-containing compound metabolic process
GO:0006810 transport
GO:0015860 purine nucleoside transmembrane transport
GO:0055085 transmembrane transport
GO:1901642 nucleoside transmembrane transport
Cellular Component
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0016020 membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway
Transport of vitamins, nucleosides, and related molecules pathway
Transmembrane transport of small molecules pathway
SLC-mediated transmembrane transport pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt O43868
TrEMBL
UniProt Splice Variant
Entrez Gene 9153
UniGene Hs.367833
RefSeq NM_004212
HUGO HGNC:11002
OMIM 606208
CCDS CCDS10121
HPRD 07069
IMGT
EMBL AF036109 AK291974 BC093737 U84392
GenPept AAB88539 AAC51930 AAH93737 BAF84663
RNA Seq Atlas 9153