Gene Gene information from NCBI Gene database.
Entrez ID 6518
Gene name Solute carrier family 2 member 5
Gene symbol SLC2A5
Synonyms (NCBI Gene)
GLUT-5GLUT5
Chromosome 1
Chromosome location 1p36.23
Summary The protein encoded by this gene is a fructose transporter responsible for fructose uptake by the small intestine. The encoded protein also is necessary for the increase in blood pressure due to high dietary fructose consumption. [provided by RefSeq, Jun
miRNA miRNA information provided by mirtarbase database.
91
miRTarBase ID miRNA Experiments Reference
MIRT021373 hsa-miR-9-5p Microarray 17612493
MIRT692267 hsa-miR-6815-5p HITS-CLIP 23313552
MIRT692266 hsa-miR-6865-5p HITS-CLIP 23313552
MIRT692265 hsa-miR-383-3p HITS-CLIP 23313552
MIRT692264 hsa-miR-3184-5p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
38
GO ID Ontology Definition Evidence Reference
GO:0003044 Process Regulation of systemic arterial blood pressure mediated by a chemical signal IEA
GO:0003044 Process Regulation of systemic arterial blood pressure mediated by a chemical signal ISS
GO:0005353 Function Fructose transmembrane transporter activity IBA
GO:0005353 Function Fructose transmembrane transporter activity IDA 8333543, 28083649, 29548810
GO:0005353 Function Fructose transmembrane transporter activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
138230 11010 ENSG00000142583
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P22732
Protein name Solute carrier family 2, facilitated glucose transporter member 5 (Fructose transporter) (Glucose transporter type 5, small intestine) (GLUT-5)
Protein function Functions as a fructose transporter that has only low activity with other monosaccharides (PubMed:16186102, PubMed:17710649, PubMed:28083649, PubMed:29548810, PubMed:8333543). Can mediate the uptake of 2-deoxyglucose, but with low efficiency (Pu
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00083 Sugar_tr 20 475 Sugar (and other) transporter Family
Tissue specificity TISSUE SPECIFICITY: Detected in skeletal muscle, and in jejunum brush border membrane and basolateral membrane (at protein level) (PubMed:7619085). Expressed in small intestine, and at much lower levels in kidney, skeletal muscle, and adipose tissue. {ECO
Sequence
Sequence length 501
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Carbohydrate digestion and absorption   Neutrophil degranulation
Intestinal hexose absorption
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
Long QT syndrome association rs779760381 RCV000190149
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 29642606
Adenocarcinoma of Lung Associate 34604392
Alcoholism Associate 18190912
Breast Neoplasms Associate 27074918, 29642606, 34064801, 38019251, 8700847
Calcinosis Cutis Stimulate 10622535
Carcinogenesis Associate 35813468
Carcinoma Pancreatic Ductal Associate 37738413
Cardiovascular Diseases Associate 23341889
Colorectal Neoplasms Associate 34052986
Dermatofibrosarcoma Associate 35441365