Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6518
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 2 member 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC2A5
Synonyms (NCBI Gene) Gene synonyms aliases
GLUT-5, GLUT5
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.23
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
138230 11010 ENSG00000142583
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Long QT Syndrome long qt syndrome N/A N/A ClinVar
Associations from Text Mining Disease 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