Gene Gene information from NCBI Gene database.
Entrez ID 10050
Gene name Solute carrier family 17 member 4
Gene symbol SLC17A4
Synonyms (NCBI Gene)
KAIA2138
Chromosome 6
Chromosome location 6p22.2
Summary Phosphate homeostasis is maintained by regulating intake, intestinal absorption, bone deposition and resorption, and renal excretion of phosphate. The central molecule in the control of phosphate excretion from the kidney is the sodium/phosphate cotranspo
miRNA miRNA information provided by mirtarbase database.
45
miRTarBase ID miRNA Experiments Reference
MIRT022042 hsa-miR-128-3p Microarray 17612493
MIRT1353414 hsa-miR-320a CLIP-seq
MIRT1353415 hsa-miR-320b CLIP-seq
MIRT1353416 hsa-miR-320c CLIP-seq
MIRT1353417 hsa-miR-320d CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
GO ID Ontology Definition Evidence Reference
GO:0005436 Function Sodium:phosphate symporter activity IEA
GO:0005436 Function Sodium:phosphate symporter activity TAS 10319585
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS 10319585
GO:0006796 Process Phosphate-containing compound metabolic process TAS 10319585
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604216 10932 ENSG00000146039
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y2C5
Protein name Probable small intestine urate exporter (Solute carrier family 17 member 4)
Protein function Acts as a membrane potential-dependent organic anion transporter, the transport requires a low concentration of chloride ions (PubMed:22460716). Mediates chloride-dependent transport of urate (PubMed:22460716). Mediates sodium-independent high a
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 43 444 Major Facilitator Superfamily Family
Tissue specificity TISSUE SPECIFICITY: Abundantly expressed in pancreas, liver, colon and small intestine, less in kidney. Not detected in the adrenal glands, brain, placenta, heart, testis, skeletal muscle, and lungs. {ECO:0000269|PubMed:10319585, ECO:0000269|PubMed:224607
Sequence
Sequence length 497
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Clear cell carcinoma of kidney Uncertain significance rs376955338 RCV005929132
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Atherosclerosis Associate 24951662
Gout Associate 22541845, 28252667
Hyperuricemia Associate 28252667
Neoplasms Associate 36325340
Prostatic Neoplasms Associate 36325340