Homo sapiens Gene: SLC23A1
Summary
InnateDB Gene IDBG-47666.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC23A1
Gene Name solute carrier family 23 (nucleobase transporters), member 1
Synonyms SLC23A2; SVCT1; YSPL3
Species Homo sapiens
Ensembl Gene ENSG00000170482
Encoded Proteins
solute carrier family 23 (nucleobase transporters), member 1
solute carrier family 23 (nucleobase transporters), member 1
solute carrier family 23 (nucleobase transporters), member 1
solute carrier family 23 (nucleobase transporters), member 1
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 transporters. The encoded protein is active in bulk vitamin C transport involving epithelial surfaces. Previously, this gene had an official symbol of SLC23A2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:139367196-139384553
Strand Reverse strand
Band q31.2
Transcripts
ENST00000353963 ENSP00000302851
ENST00000348729 ENSP00000302701
ENST00000504513 ENSP00000422688
ENST00000506512
ENST00000503919
ENST00000502863
ENST00000508270 ENSP00000427271
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [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:0005515 protein binding
GO:0008520 L-ascorbate:sodium symporter activity
GO:0015081 sodium ion transmembrane transporter activity
GO:0015205 nucleobase transmembrane transporter activity
GO:0015229 L-ascorbic acid transporter activity
GO:0033300 dehydroascorbic 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:0007420 brain development
GO:0009636 response to toxic substance
GO:0015851 nucleobase transport
GO:0015882 L-ascorbic acid transport
GO:0019852 L-ascorbic acid metabolic process
GO:0030324 lung development
GO:0035461 vitamin transmembrane transport
GO:0035725 sodium ion transmembrane transport
GO:0044281 small molecule metabolic process
GO:0055085 transmembrane transport
GO:0070837 dehydroascorbic acid 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:0005903 brush border
GO:0009925 basal plasma membrane
GO:0016020 membrane
GO:0016324 apical plasma membrane
GO:0043229 intracellular organelle
GO:0070062 extracellular vesicular exosome
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 H0YAJ1
UniProt Splice Variant
Entrez Gene 9963
UniGene Hs.643467 Hs.739242
RefSeq NM_005847 NM_152685 XM_005272148 XM_005272149
HUGO HGNC:10974
OMIM 603790
CCDS CCDS4212 CCDS4213
HPRD 04810
IMGT
EMBL AC135457
GenPept
RNA Seq Atlas 9963