SULT1A2

Gene Name		sulfotransferase family, cytosolic, 1A, phenol-preferring, member 2
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Gene Ontology Annotations	Cellular Component	Cytosol
	Molecular Function	Aryl Sulfotransferase Activity Sulfotransferase Activity Flavonol 3-sulfotransferase Activity
	Biological Process	Catecholamine Metabolic Process Xenobiotic Metabolic Process Steroid Metabolic Process Amine Biosynthetic Process Phenol-containing Compound Metabolic Process Small Molecule Metabolic Process 3'-phosphoadenosine 5'-phosphosulfate Metabolic Process Sulfation
Pathways		Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD) Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Defective UGT1A4 causes hyperbilirubinemia Metabolic disorders of biological oxidation enzymes Phase II conjugation Defective UGT1A1 causes hyperbilirubinemia Cytosolic sulfonation of small molecules Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) Biological oxidations Defective GGT1 causes Glutathionuria (GLUTH) Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Defective GSS causes Glutathione synthetase deficiency (GSS deficiency)
Drugs
Diseases
GWAS		Body mass index ( 20935630) Inflammatory bowel disease ( 23128233) Inflammatory bowel disease (early onset) ( 19915574)
Protein-protein Interactions		1 interactors: NIF3L1
Entrez ID		6799
HPRD ID		03187
Ensembl ID		ENSG00000197165
Uniprot IDs		P50226
PDB IDs		1Z29
Enriched GO Terms of Interacting Partners?		7,8-dihydroneopterin 3'-triphosphate Biosynthetic Process Dihydrobiopterin Metabolic Process Pteridine-containing Compound Biosynthetic Process Pteridine-containing Compound Metabolic Process
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