Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10050
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 17 member 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC17A4
Synonyms (NCBI Gene) Gene synonyms aliases
KAIA2138
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p22.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005436 Function Sodium:phosphate symporter activity TAS 10319585
GO:0005764 Component Lysosome IBA 21873635
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0006796 Process Phosphate-containing compound metabolic process TAS 10319585
GO:0006814 Process Sodium ion transport TAS 10319585
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604216 10932 ENSG00000146039
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Lung carcinoma Carcinoma of lung rs1805076, rs121909071, rs121913530, rs112445441, rs121913529, rs121913535, rs121913297, rs121913279, rs104886003, rs397516975, rs11554290, rs121913364, rs121913351, rs121913369, rs121913355
View all (44 more)
28604730
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
30285260
Unknown
Disease term Disease name Evidence References Source
Atherosclerosis Atherosclerosis 21909108 ClinVar
Coronary heart disease Coronary heart disease 21971053 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Atherosclerosis Associate 24951662
Gout Associate 22541845, 28252667
Hyperuricemia Associate 28252667
Neoplasms Associate 36325340
Prostatic Neoplasms Associate 36325340