SLC5A1

Description		solute carrier family 5 member 1
Image		No pdb structure
GO Annotations	Cellular Component	Early Endosome Plasma Membrane Integral Component Of Plasma Membrane Cell-cell Junction Integral Component Of Membrane Apical Plasma Membrane Brush Border Membrane Intracellular Organelle Perinuclear Region Of Cytoplasm Extracellular Exosome Intracellular Vesicle
	Molecular Function	Galactose Transmembrane Transporter Activity Glucose Transmembrane Transporter Activity Myo-inositol:sodium Symporter Activity Water Transmembrane Transporter Activity Glucose:sodium Symporter Activity Protein Binding Pentose Transmembrane Transporter Activity Fucose Transmembrane Transporter Activity Alpha-glucoside Transmembrane Transporter Activity D-glucose Transmembrane Transporter Activity
	Biological Process	Alpha-glucoside Transport Sodium Ion Transport Response To Inorganic Substance Pentose Transmembrane Transport Fucose Transmembrane Transport Galactose Transmembrane Transport Myo-inositol Transport Transepithelial Water Transport Glucose Import Across Plasma Membrane Sodium Ion Import Across Plasma Membrane Intestinal Hexose Absorption Transport Across Blood-brain Barrier Chloride Transmembrane Transport Glucose Transmembrane Transport
Pathways		Cellular hexose transport Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM) Intestinal hexose absorption
Drugs
Diseases
GWAS		1,5-anhydroglucitol levels ( 28588231) GIP levels in response to oral glucose tolerance test (120 minutes) ( 29093273) GLP-1 levels in response to oral glucose tolerance test (120 minutes) ( 29093273)
Interacting Genes		1 interacting genes: HSPA1A
Entrez ID		6523
HPRD ID		01668
Ensembl ID		ENSG00000100170
Uniprot IDs		P13866
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?