SLC16A1

Description		solute carrier family 16 member 1
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GO Annotations	Cellular Component	Centrosome Plasma Membrane Integral Component Of Plasma Membrane Basal Plasma Membrane Membrane Integral Component Of Membrane Basolateral Plasma Membrane Apical Plasma Membrane Lateral Plasma Membrane Cell Junction Intracellular Membrane-bounded Organelle Synapse Extracellular Exosome
	Molecular Function	Protein Binding Monocarboxylic Acid Transmembrane Transporter Activity Lactate Transmembrane Transporter Activity Mevalonate Transmembrane Transporter Activity Symporter Activity Identical Protein Binding Carboxylic Acid Transmembrane Transporter Activity Organic Cyclic Compound Binding
	Biological Process	Lipid Metabolic Process Centrosome Cycle Monocarboxylic Acid Transport Mevalonate Transport Response To Food Plasma Membrane Lactate Transport Glucose Homeostasis Regulation Of Insulin Secretion Behavioral Response To Nutrient Cellular Response To Organic Cyclic Compound Transport Across Blood-brain Barrier Carboxylic Acid Transmembrane Transport
Pathways		Basigin interactions Proton-coupled monocarboxylate transport Defective SLC16A1 causes symptomatic deficiency in lactate transport (SDLT) Pyruvate metabolism
Drugs		Pyruvic acid Mersalyl
Diseases
GWAS		Macular thickness ( 30535121) Proportion of activated microglia (inferior temporal cortex) ( 30679421) Refractive error ( 32231278)
Interacting Genes		3 interacting genes: AGTR1 BSG CRBN
Entrez ID		6566
HPRD ID		02816
Ensembl ID		ENSG00000155380
Uniprot IDs		A0A024R0H1 B4DKS0 P53985
PDB IDs		6LYY 6LZ0 7CKO 7CKR 7DA5
Enriched GO Terms of Interacting Partners?
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