Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
115584
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 5 member 11
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC5A11
Synonyms (NCBI Gene) Gene synonyms aliases
KST1, RKST1, SGLT6, SMIT2
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16p12.1
Summary Summary of gene provided in NCBI Entrez Gene.
Cotransporters, such as SLC5A11, represent a major class of proteins that make use of ion gradients to drive active transport for the cellular accumulation of nutrients, neurotransmitters, osmolytes, and ions Roll et al. (2002) [PubMed 12039040].[supplied
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT2332165 hsa-miR-4694-3p CLIP-seq
MIRT2332166 hsa-miR-4709-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005412 Function Glucose:sodium symporter activity IBA 21873635
GO:0005515 Function Protein binding IPI 25416956
GO:0005886 Component Plasma membrane IBA 21873635
GO:0005886 Component Plasma membrane TAS
GO:0006814 Process Sodium ion transport IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610238 23091 ENSG00000158865
Protein
UniProt ID Q8WWX8
Protein name Sodium/myo-inositol cotransporter 2 (Na(+)/myo-inositol cotransporter 2) (Sodium-dependent glucose cotransporter) (Sodium/glucose cotransporter KST1) (Sodium/myo-inositol transporter 2) (SMIT2) (Solute carrier family 5 member 11)
Protein function Involved in the sodium-dependent cotransport of myo-inositol (MI) with a Na(+):MI stoichiometry of 2:1 (PubMed:15172003, PubMed:19032932). Exclusively responsible for apical MI transport and absorption in intestine (By similarity). Can also tran
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00474 SSF 58 487 Sodium:solute symporter family Family
Tissue specificity TISSUE SPECIFICITY: Highest expression in heart, skeletal muscle, kidney, liver and placenta. Weaker expression in brain, colon, spleen, lung and peripheral blood leukocytes. {ECO:0000269|PubMed:12039040}.
Sequence
Sequence length 675
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Inositol transporters
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Gout Gout GWAS
Associations from Text Mining
Disease Name Relationship Type References
Cerebral Infarction Associate 26352407
Hypertension Pulmonary Associate 26352407
Obesity Associate 34207686
Renal Insufficiency Chronic Associate 26352407
Thyroid Carcinoma Anaplastic Associate 26680454