Showing entry for UDP-glucuronosyltransferase 1-3


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT009840
Protein NameUDP-glucuronosyltransferase 1-3
Uniport IdP35503
GeneUGT1A3
Gene Id54659
DomainUDPGT
Pfam PF00201  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
1. Metabolism 1.1 Carbohydrate metabolism hsa00040 Pentose and glucuronate interconversions
1. Metabolism 1.1 Carbohydrate metabolism hsa00053 Ascorbate and aldarate metabolism
1. Metabolism 1.3 Lipid metabolism hsa00140 Steroid hormone biosynthesis
1. Metabolism 1.8 Metabolism of cofactors and vitamins hsa00830 Retinol metabolism
1. Metabolism 1.8 Metabolism of cofactors and vitamins hsa00860 Porphyrin and chlorophyll metabolism
1. Metabolism 1.11 Xenobiotics biodegradation and metabolism hsa00980 Metabolism of xenobiotics by cytochrome P450
1. Metabolism 1.11 Xenobiotics biodegradation and metabolism hsa00982 Drug metabolism - cytochrome P450
1. Metabolism 1.11 Xenobiotics biodegradation and metabolism hsa00983 Drug metabolism - other enzymes
1. Metabolism 1.0 Global and overview maps hsa01100 Metabolic pathways
6. Human Diseases 6.1 Cancers: Overview hsa05204 Chemical carcinogenesis
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0052695 cellular glucuronidation
Biological Process GO:0052696 flavonoid glucuronidation
Biological Process GO:2001030 negative regulation of cellular glucuronidation
Biological Process GO:0045922 negative regulation of fatty acid metabolic process
Biological Process GO:1904224 negative regulation of glucuronosyltransferase activity
Biological Process GO:0042573 retinoic acid metabolic process
Biological Process GO:0052697 xenobiotic glucuronidation
molecular function GO:0019899 enzyme binding
molecular function GO:0015020 glucuronosyltransferase activity
molecular function GO:0046982 protein heterodimerization activity
molecular function GO:0042803 protein homodimerization activity
molecular function GO:0001972 retinoic acid binding
cellular component GO:0005783 endoplasmic reticulum
cellular component GO:0005789 endoplasmic reticulum membrane
cellular component GO:0016021 integral component of membrane
Reactome
Pathway Id Pathway Name
R-HSA-1430728 Metabolism
R-HSA-156580 Phase II - Conjugation of compounds
R-HSA-156588 Glucuronidation
R-HSA-162582 Signal Transduction
R-HSA-211859 Biological oxidations
R-HSA-9006931 Signaling by Nuclear Receptors
R-HSA-9024446 NR1H2 and NR1H3-mediated signaling
R-HSA-9623433 NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0002875 BXGD000135 Cooley's anemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0002895 BXGD000152 Anemia, Sickle Cell Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0004096 BXGD000252 Asthma Respiratory Tract Diseases; Immune System Diseases
C0005283 BXGD000308 beta Thalassemia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007097 BXGD000424 Carcinoma Neoplasms
C0008350 BXGD000531 Cholelithiasis Digestive System Diseases
C0008370 BXGD000534 Cholestasis Digestive System Diseases
C0010324 BXGD000663 Crigler Najjar syndrome, type 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0010414 BXGD000669 Infection by Cryptococcus neoformans Infections
C0011226 BXGD000704 Hepatitis D Infection Digestive System Diseases; Infections
C0011860 BXGD000755 Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases; Endocrine System Diseases
C0014544 BXGD000926 Epilepsy Nervous System Diseases
C0017205 BXGD001105 Gaucher Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0017551 BXGD001116 Gilbert Disease (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0017921 BXGD001152 Glycogen storage disease type II Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0020433 BXGD001379 Hyperbilirubinemia Pathological Conditions, Signs and Symptoms
C0021400 BXGD001504 Influenza Infections; Respiratory Tract Diseases
C0022346 BXGD001537 Icterus Pathological Conditions, Signs and Symptoms
C0023530 BXGD001683 Leukopenia Hemic and Lymphatic Diseases
C0023895 BXGD001717 Liver diseases Digestive System Diseases
C0027651 BXGD002009 Neoplasms Neoplasms
C0027947 BXGD002061 Neutropenia Hemic and Lymphatic Diseases
C0028754 BXGD002082 Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0032580 BXGD002362 Adenomatous Polyposis Coli Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C0036341 BXGD002600 Schizophrenia Mental Disorders
C0036572 BXGD002625 Seizures Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0152013 BXGD003516 Adenocarcinoma of lung (disorder) Neoplasms
C0202117 BXGD004074 Low density lipoprotein cholesterol measurement
C0202236 BXGD004086 Triglycerides measurement
C0235974 BXGD004796 Pancreatic carcinoma Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0268138 BXGD005833 Xeroderma Pigmentosum, Complementation Group D Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0268306 BXGD005891 Unconjugated hyperbilirubinemia Pathological Conditions, Signs and Symptoms
C0270210 BXGD006068 Lucey-Driscoll syndrome (disorder) Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0271979 BXGD006283 Thalassemia Intermedia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0311468 BXGD006885 Increased bilirubin level (finding) Pathological Conditions, Signs and Symptoms
C0334294 BXGD007025 Multiple adenomatous polyps Neoplasms
C0337438 BXGD007159 Glucose measurement
C0342751 BXGD007542 Generalized glycogen storage disease of infants Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0344395 BXGD007668 Bilirubin measurement
C0346647 BXGD007832 Malignant neoplasm of pancreas Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0376154 BXGD007980 Skin callus Skin and Connective Tissue Diseases
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0428474 BXGD008631 Serum LDL cholesterol measurement
C0489786 BXGD009018 Height
C0495706 BXGD009038 elevated blood glucose level
C0523465 BXGD009209 Serum albumin measurement
C0524620 BXGD009236 Metabolic Syndrome X Nutritional and Metabolic Diseases
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0741494 BXGD010035 Elevated total bilirubin
C0857007 BXGD011131 Hyperbilirubinemia, Neonatal Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0947622 BXGD011493 Cholecystolithiasis Digestive System Diseases
C1287365 BXGD012174 Bilirubin level result
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1314665 BXGD012386 Serum alkaline phosphatase raised
C1337013 BXGD012876 Differentiated Thyroid Gland Carcinoma
C1445957 BXGD013081 Serum total cholesterol measurement
C1611743 BXGD013456 Familial (FPAH)
C1859236 BXGD015867 Prolonged neonatal jaundice Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C1866173 BXGD016380 BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
C2931132 BXGD017963 Crigler Najjar syndrome, type 2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C2985280 BXGD018223 Blood Protein Measurement
C4303163 BXGD022553 Autoimmune hepatitis type 2
C4721579 BXGD023759 Secondary malignant neoplasm of colon and/or rectum Digestive System Diseases; Neoplasms
C4722172 BXGD023791 Primary differentiated carcinoma of thyroid gland
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000130 Estradiol 272.38
BXGC0000332 Fisetin 286.24
BXGC0000363 Galangin 270.24
BXGC0000383 (S)-Naringenin 272.25
BXGC0000663 Papain 206.28
BXGC0000681 Umbelliferone 162.14
BXGC0001550 Ficus Latex peptide 2 244.26
BXGC0001778 Scutellarein 286.24
BXGC0002052 Aesculetin 178.14
BXGC0002071 Apigenin 270.24
BXGC0002248 Dodecanoic acid 200.32
BXGC0003485 Naphthalen-1-ol 144.17
BXGC0003949 Thymunic acid 150.22
BXGC0004378 3-Hydroxyflavone 238.24
BXGC0004705 Diphenylamine 169.22
BXGC0004719 2-Biphenylol 170.21
BXGC0005683 Quercetin 302.24
BXGC0005771 Decanoic acid 172.26
BXGC0005870 Codeine 299.36
BXGC0005879 Eugenol 164.2
BXGC0006276 Tigogenin 416.64
BXGC0006291 Scopoletin 192.17
BXGC0007029 Emodin 270.24
BXGC0007528 p-Menthan-3-ol 156.27
BXGC0013544 Naphthalen-1-Amine 143.07
BXGC0016891 Nortriptyline 263.17
BXGC0017965 4-Hydroxycoumarins 162.03
BXGC0018843 Quinalizarin 272.03
BXGC0022978 Biphenyl-4-Amine 169.09
BXGC0025066 Benzidine 184.1
BXGC0026391 Naloxone 327.15
BXGC0030901 Morphine 285.14
BXGC0032207 Disogenin 414.31
BXGC0032351 Nalorphine 311.15
BXGC0035676 morphine-3-glucuronide 461.17
BXGC0037915 isoborneol 154.14
BXGC0039397 Athraquinones A 240.04
BXGC0044334 P-Nitrophenol 139.03
BXGC0045812 Trifluoperazine 407.16
BXGC0047169 Hymecromone 176.05
BXGC0049738 Dexibuprofen 206.13
BXGC0052021 (R)-Ibuprophen 206.13
BXGC0052712 Anthraflavicacid 240.04
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein