Homo sapiens Gene: SLC23A2
Summary
InnateDB Gene IDBG-50310.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC23A2
Gene Name solute carrier family 23 (nucleobase transporters), member 2
Synonyms NBTL1; SLC23A1; SVCT2; YSPL2
Species Homo sapiens
Ensembl Gene ENSG00000089057
Encoded Proteins
solute carrier family 23 (nucleobase transporters), member 2
solute carrier family 23 (nucleobase transporters), member 2
solute carrier family 23 (nucleobase transporters), member 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 20:4852356-5010293
Strand Reverse strand
Band p13
Transcripts
ENST00000379333 ENSP00000368637
ENST00000338244 ENSP00000344322
ENST00000423430 ENSP00000396364
ENST00000468355
ENST00000496331
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005215 transporter activity
GO:0008520 L-ascorbate:sodium symporter activity
GO:0008523 sodium-dependent multivitamin transmembrane transporter activity
GO:0015205 nucleobase transmembrane transporter activity
GO:0015229 L-ascorbic acid transporter activity
GO:0070890 sodium-dependent L-ascorbate transmembrane transporter activity
Biological Process
GO:0006139 nucleobase-containing compound metabolic process
GO:0006766 vitamin metabolic process
GO:0006767 water-soluble vitamin metabolic process
GO:0006810 transport
GO:0006814 sodium ion transport
GO:0006979 response to oxidative stress
GO:0015851 nucleobase transport
GO:0015882 L-ascorbic acid transport
GO:0015993 molecular hydrogen transport
GO:0019852 L-ascorbic acid metabolic process
GO:0035461 vitamin transmembrane transport
GO:0044281 small molecule metabolic process
GO:0055085 transmembrane transport
GO:0070904 transepithelial L-ascorbic acid transport
Cellular Component
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0009925 basal plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016323 basolateral plasma membrane
GO:0016324 apical plasma membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Vitamin C (ascorbate) metabolism pathway
Defective HLCS causes multiple carboxylase deficiency pathway
Defective MUT causes methylmalonic aciduria mut type pathway
Defective MMAA causes methylmalonic aciduria type cblA pathway
Defective TCN2 causes hereditary megaloblastic anemia pathway
Metabolism of water-soluble vitamins and cofactors pathway
Defective AMN causes hereditary megaloblastic anemia 1 pathway
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG pathway
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF pathway
Defective CD320 causes methylmalonic aciduria pathway
Defects in cobalamin (B12) metabolism pathway
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC pathway
Defects in biotin (Btn) metabolism pathway
Defective BTD causes biotidinase deficiency pathway
Defective GIF causes intrinsic factor deficiency pathway
Defects in vitamin and cofactor metabolism pathway
Defective CUBN causes hereditary megaloblastic anemia 1 pathway
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD pathway
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE pathway
Metabolism pathway
Defective MMAB causes methylmalonic aciduria type cblB pathway
Disease pathway
Metabolism of vitamins and cofactors pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.516866 Hs.594775 Hs.736328
RefSeq NM_005116 NM_203327 XM_005260904 XM_006723671
HUGO
OMIM
CCDS CCDS13085
HPRD 04811
IMGT
EMBL
GenPept
RNA Seq Atlas