SLC2A1

Description		solute carrier family 2 member 1
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GO Annotations	Cellular Component	Golgi Membrane Female Pronucleus Cytosol Plasma Membrane Integral Component Of Plasma Membrane Caveola Intercalated Disc Membrane Basolateral Plasma Membrane Apical Plasma Membrane Z Disc Midbody Cortical Actin Cytoskeleton Sarcolemma Melanosome Extracellular Exosome Blood Microparticle Presynapse
	Molecular Function	Glucose Transmembrane Transporter Activity Protein Binding Kinase Binding Dehydroascorbic Acid Transmembrane Transporter Activity Identical Protein Binding Xenobiotic Transmembrane Transporter Activity Protein Self-association D-glucose Transmembrane Transporter Activity
	Biological Process	Response To Hypoxia Lactose Biosynthetic Process Female Pregnancy Regulation Of Glucose Transmembrane Transport L-ascorbic Acid Metabolic Process Cerebral Cortex Development Response To Insulin Cellular Response To Glucose Starvation Xenobiotic Transport Regulation Of Insulin Secretion Protein-containing Complex Assembly Dehydroascorbic Acid Transport Cellular Response To Mechanical Stimulus Cellular Hyperosmotic Response Response To Thyroglobulin Triiodothyronine Glucose Transmembrane Transport
Pathways		Cellular hexose transport Vitamin C (ascorbate) metabolism Regulation of insulin secretion Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1) Lactose synthesis
Drugs		Resveratrol
Diseases		GLUT1 deficiency syndrome (GLUT1DS); Glucose transport defect of the blood-brain barrier Primary torsion dystonia (PTD)
GWAS		Birth weight ( 31043758) Cardiac hypertrophy ( 21348951) Monocyte count ( 27863252) Pre-treatment viral load in HIV-1 infection ( 31219150)
Interacting Genes		13 interacting genes: CALR CANX COPS6 GAPDH GIPC1 HSPB2 PDIA3 PTK2B SNX27 STOM SUMO1 UBE2I VHL
Entrez ID		6513
HPRD ID		00683
Ensembl ID		ENSG00000117394
Uniprot IDs		P11166 Q59GX2
PDB IDs		1SUK 4PYP 5EQG 5EQH 5EQI
Enriched GO Terms of Interacting Partners?
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