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SLC23A3 (solute carrier family 23 member 3)
Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
151295
Gene nameGene Name - the full gene name approved by the HGNC.
Solute carrier family 23 member 3
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
SLC23A3
SynonymsGene synonyms aliases
E2BP3, SVCT3, Yspl1
ChromosomeChromosome number
2
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q35
miRNAmiRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
miRTarBase ID miRNA Experiments Reference
MIRT609954 hsa-miR-8485 HITS-CLIP 23824327
MIRT609953 hsa-miR-329-3p HITS-CLIP 23824327
MIRT609952 hsa-miR-362-3p HITS-CLIP 23824327
MIRT609951 hsa-miR-603 HITS-CLIP 23824327
MIRT609950 hsa-miR-4789-3p HITS-CLIP 23824327
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
GO ID Ontology Definition Evidence Reference
GO:0005215 Function Transporter activity IBA 21873635
GO:0016021 Component Integral component of membrane IEA
GO:0022857 Function Transmembrane transporter activity IEA
GO:0055085 Process Transmembrane transport IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM
HGNC
e!Ensembl
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q6PIS1
Protein name Solute carrier family 23 member 3 (HPC E2-binding protein 3) (Na(+)/L-ascorbic acid transporter 3) (Sodium-dependent vitamin C transporter 3)
Protein function Acts as a sodium-dependent hypoxanthine transporter (PubMed:35094660). May show xanthine-hypoxanthine exchange activity (PubMed:35094660).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00860 Xan_ur_permease
47 → 473
Permease family
 Family
Sequence
Sequence length 610
Interactions View interactions
Associated diseases
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Causal
Disease name Disease term dbSNP ID References
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 23474461

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