SLC17A2 (solute carrier family 17 member 2)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10246
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 17 member 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC17A2
Synonyms (NCBI Gene) Gene synonyms aliases
NPT3
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p22.2
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(5)
miRTarBase ID miRNA Experiments Reference
MIRT019007 hsa-miR-335-5p Microarray 18185580
MIRT1353410 hsa-miR-185 CLIP-seq
MIRT1353411 hsa-miR-4306 CLIP-seq
MIRT1353412 hsa-miR-4644 CLIP-seq
MIRT1353413 hsa-miR-4802-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(12)
GO ID Ontology Definition Evidence Reference
GO:0005436 Function Sodium:phosphate symporter activity TAS 9149941
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 9149941
GO:0006814 Process Sodium ion transport TAS 9149941
Other IDs Other 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
611049 10930 ENSG00000112337
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID O00624
Protein name Sodium-dependent phosphate transport protein 3 (Na(+)/PI cotransporter 3) (Sodium/phosphate cotransporter 3) (Solute carrier family 17 member 2)
Protein function Acts as a membrane potential-dependent organic anion transporter, the transport requires a low concentration of chloride ions (By similarity). Mediates chloride-dependent transport of urate (By similarity). Can actively transport inorganic phosp
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 24 → 425 Major Facilitator Superfamily Family
Tissue specificity TISSUE SPECIFICITY: Expressed in the small intestine, kidney, spleen and testis. Not detected in fetal brain, bone marrow, and mammary gland. {ECO:0000269|PubMed:9149941}.
Sequence
Sequence length 439
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (3)
Unknown
Disease term Disease name Evidence References Source
Systemic lupus erythematosus Systemic lupus erythematosus GWAS
Psoriasis Psoriasis GWAS
Dental caries Dental caries GWAS
Show/Hide Text Mining Associations (5)
Associations from Text Mining
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 29482039
Dental Plaque Associate 29482039
Gout Associate 29497127
Personality Disorders Associate 33450964
Prostatic Neoplasms Associate 33450964