191321
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UDP glucuronosyltransferase family 1 member A1 |
BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT 1-1, UGT1, UGT1A |
Curated: Autism, Serum bilirubin level, Bile duct calculus, Small cell carcinoma, Cholecystolithiasis, Contact dermatitis, Crigler-najjar syndrome, Crohn disease, Gallstones, Gilbert syndrome, Hodgkin disease, Hyperbilirubinemia, Insomnia, Kidney failure, Lucey-driscoll syndrome, Neutropenia, Perinatal disease, Neonatal hyperbilirubinemia
Unreviewed: Acromegaly, Acute Kidney Insufficiency, Adenocarcinoma, Adenocarcinoma Of Colon, Adenoma, Adrenoleukodystrophy, Allergic Sensitization, alpha Thalassemia, Anemia, Asthenia, Asthma, Autism spectrum disorder, Benign Prostatic Hyperplasia, beta Thalassemia, Bile duct disease, Biliary Tract Cancer, Biliary tract neoplasms, Bladder carcinoma, Bladder Neoplasm, Bone marrow diseases, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchopulmonary Dysplasia, Carcinogenesis, Carcinoid tumor, Carcinoma, Cardiovascular Diseases, Carney Complex, Cerebral palsy, Cerebrovascular Disorders, Cholangiocarcinoma, Choledocholithiasis, Cholelithiasis, Cholestasis, Cholesterol gallstones, Classical Hodgkin lymphoma, Colon Carcinoma, Colonic neoplasm, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital Chromosomal Disease, Congenital dyserythropoietic anemia, Congenital heart defect, Congenital heart septal defect, Congenital hypertrophic pyloric stenosis, Congestive Heart Failure, Conotruncal cardiac defect, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Crigler-Najjar syndrome, Crohn Disease, Cyclic Neutropenia, Cystic Fibrosis, Deficiency Of Glucose-6-Phosphate Dehydrogenase, Dermatitis, Developmental Delay, Developmental disability, Diabetes Mellitus, Diabetes mellitus, type 2, Diarrhea, Dyslipidemias, Endometrial Cancer, Endometrial carcinoma, Endometrial neoplasm, Endometrial Neoplasms, Endometrioid carcinoma, Endometriosis, Epilepsy, Epileptic encephalopathy, Epithelial ovarian carcinoma, Esophageal Cancer, Esophageal Carcinoma, Esophageal neoplasm, Esophagus Neoplasm, Fabry disease, Fatty liver, Galactosemia, Gastrointestinal disease, Gastrointestinal neoplasm, Gastroschisis, Gaucher Disease, Gilbert Disease, Glioma, Glycogen Storage Disease, Graves Disease, Head and neck cancer, Head And Neck Carcinoma, Hearing loss, Heart Failure, Hematologic disease, Hemoglobinopathy, Hemolysis, Hemolytic anemia, Hepatitis c, Hepatocellular carcinoma, Hepatolenticular degeneration, Hereditary angioedema, Hereditary Hemochromatosis, Hereditary Spherocytosis, Hodgkin Disease, Hodgkin Lymphoma, Hodgkin Lymphoma, Lymphocyte Depletion, Huntington Disease, Hypercholesterolemia, Hyperinsulinism, Hyperprolactinemia, Hypersensitivity, Hypertension, Hypoglycemia, Inflammatory Bowel Disease, Iron Overload, Ischemic Stroke, Kernicterus, Kidney Cancer, Kidney Disease, Kidney Failure, Kidney neoplasm, Kidney stone, Laryngeal Carcinoma, Laryngeal neoplasm, Larynx cancer, Leukemia, LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS, Leukopenia, Lichen amyloidosis, Liver Cancer, Liver carcinoma, Liver failure, Liver Fibrosis, Lucey-Driscoll syndrome, Lung Cancer, Lung carcinoma, Lung disease, Lung neoplasms, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Malignant gastrointestinal tract tumors, Malignant Neoplasm, Malignant Neoplasm Of Testis, Malignant testicular germ cell tumor, Mammary Neoplasms, Mental retardation, Metabolic Diseases, Metabolic Syndrome, Monocytic Leukemia, Mucositis, Multiple sclerosis, Multiple Trichoepithelioma, Myeloblastic Leukemia, Myeloid Leukemia, Myocardial Infarction, Myocardial Ischemia, Nausea, Neoplasms, Nephrolithiasis, Neurodevelopmental Disorders, Non-Alcoholic Fatty Liver Disease, Obesity, Oculocutaneous albinism, Oculomotor nerve palsy, Osteoporosis, Ovarian cancer, Ovarian Carcinoma, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Pancreatitis, Prostate cancer, Prostatic neoplasm, Pseudohyperkalemia Cardiff, Psychotic disorders, Rectal Carcinoma, Renal Carcinoma, Renal cell carcinoma, Respiration Disorders, Respiratory Distress Syndrome, Respiratory system infectious disease, Respiratory Tract Diseases, Retinoblastoma, Rheumatoid arthritis, Sarcoma, Scleroderma, Sclerosing cholangitis, Septicemia, Sickle cell anemia, Small cell lung carcinoma, Small Intestinal Carcinoma, Small intestine cancer, Spherocytosis, Spinocerebellar ataxia, Squamous cell carcinoma, Status Epilepticus, Stomach Carcinoma, Stomach Neoplasms, Stomatitis, Stroke, Thalassemia, Thrombocytopenia, Thyroid cancer, Thyroid Carcinoma, Transient Hyperbilirubinemia, Trichohepatoenteric Syndrome, Ulcerative colitis, Urinary bladder cancer, Urinary bladder neoplasms, Uterine neoplasm, Vascular Diseases, Wilms tumor, Xeroderma Pigmentosum
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191322
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UDP glucuronosyltransferase family 1 member A10 |
GNT1, UDPGT, UGT-1A, UGT-1J, UGT1, UGT1-01, UGT1-10, UGT1.1, UGT1.10, UGT1A, UGT1A1, UGT1J, hUG-BR1 |
Curated: Attention deficit hyperactivity disorder, Autism, Bilirubin metabolism disease, Cholecystolithiasis, Crigler-najjar syndrome, Melanoma, Gallstones, Gilbert syndrome, Insomnia, Alzheimer disease, Liver disease, Lucey-driscoll syndrome, Neuroblastoma, Nonalcoholic fatty liver disease, Perinatal disease, Urinary bladder cancer
Unreviewed: alpha Thalassemia, Anemia, Benign Prostatic Hyperplasia, beta Thalassemia, Bladder carcinoma, Breast Carcinoma, Breast neoplasm, Carcinoma, Cholangiocarcinoma, Cholelithiasis, Cholestasis, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Crigler-Najjar syndrome, Deficiency Of Glucose-6-Phosphate Dehydrogenase, Diabetes Mellitus, Esophageal squamous cell carcinoma, Gastroschisis, Gaucher Disease, Gilbert Disease, Glycogen Storage Disease, Hereditary Spherocytosis, Hyperbilirubinemia, Kernicterus, LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS, Leukopenia, Liver carcinoma, Lucey-Driscoll syndrome, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Metabolic Syndrome, Myeloid Leukemia, Neoplasms, Neutropenia, Non-Alcoholic Fatty Liver Disease, Obesity, Pancreatic neoplasm, Prostate cancer, Rheumatoid arthritis, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Thalassemia, Thyroid Carcinoma, Xeroderma Pigmentosum
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191323
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UDP glucuronosyltransferase family 1 member A11, pseudogene |
UGT1K |
Curated: N/A
Unreviewed: N/A
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191324
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UDP glucuronosyltransferase family 1 member A12, pseudogene |
UGT1L |
Curated: N/A
Unreviewed: N/A
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191325
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UDP glucuronosyltransferase family 1 member A13, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
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191326
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UDP glucuronosyltransferase family 1 member A2, pseudogene |
UGT1BP |
Curated: N/A
Unreviewed: N/A
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191327
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UDP glucuronosyltransferase family 1 member A3 |
UDPGT, UDPGT 1-3, UGT-1C, UGT1-03, UGT1.3, UGT1A3S, UGT1C |
Curated: Bilirubin metabolism disease, Cholecystolithiasis, Crigler-najjar syndrome, Gallstones, Gilbert syndrome, Insomnia, Liver disease, Lucey-driscoll syndrome, Nonalcoholic fatty liver disease, Perinatal disease, Schizophrenia
Unreviewed: Anemia, Asthma, beta Thalassemia, Breast Carcinoma, Breast neoplasm, Carcinoma, Cholelithiasis, Cholestasis, Colorectal neoplasm, Colorectal Neoplasms, Crigler-Najjar syndrome, Diabetes Mellitus, Epilepsy, Gastroschisis, Gaucher Disease, Gilbert Disease, Glycogen Storage Disease, Hyperbilirubinemia, Leukopenia, Lucey-Driscoll syndrome, Lung adenocarcinoma, Malignant Neoplasm, Metabolic Syndrome, Multiple polyposis syndrome, Neoplasms, Neutropenia, Obesity, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Prostate cancer, Stomach neoplasms, Thalassemia, Thyroid cancer, Thyroid Carcinoma, Urinary bladder neoplasms, Xeroderma Pigmentosum
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191328
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UDP glucuronosyltransferase family 1 member A4 |
GNT1, HUG-BR2, UDPGT, UDPGT 1-4, UGT-1A, UGT-1D, UGT1, UGT1-01, UGT1-04, UGT1.1, UGT1.4, UGT1A, UGT1A1, UGT1A4S, UGT1D, hUG-BR1 |
Curated: Bilirubin metabolism disease, Celiac disease, Cholecystolithiasis, Crigler-najjar syndrome, Gallstones, Gilbert syndrome, Insomnia, Liver disease, Lucey-driscoll syndrome, Nonalcoholic fatty liver disease, Perinatal disease
Unreviewed: alpha Thalassemia, Anemia, Benign Prostatic Hyperplasia, beta Thalassemia, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cholelithiasis, Cholestasis, Colorectal Cancer, Colorectal Neoplasms, Crigler-Najjar syndrome, Deficiency Of Glucose-6-Phosphate Dehydrogenase, Diabetes Mellitus, Epilepsy, Fleck Corneal Dystrophy, Gastroschisis, Gaucher Disease, Gilbert Disease, Glycogen Storage Disease, Hematologic neoplasm, Hematologic Neoplasms, Hepatocellular carcinoma, Hereditary Spherocytosis, Hyperbilirubinemia, Kernicterus, Leukopenia, Liver cirrhosis, Lucey-Driscoll syndrome, Malignant Neoplasm, Metabolic Syndrome, Myeloid Leukemia, Neoplasms, Neutropenia, Non-Alcoholic Fatty Liver Disease, Obesity, Prostate cancer, Rheumatoid arthritis, Stomach Carcinoma, Stomach Neoplasms, Thalassemia, Thyroid Carcinoma, Xeroderma Pigmentosum
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191329
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UDP glucuronosyltransferase family 1 member A5 |
UDPGT, UDPGT 1-5, UGT1E |
Curated: Bilirubin metabolism disease, Cholecystolithiasis, Crigler-najjar syndrome, Gallstones, Gilbert syndrome, Insomnia, Liver disease, Lucey-driscoll syndrome, Nonalcoholic fatty liver disease, Perinatal disease
Unreviewed: Anemia, beta Thalassemia, Carcinoma, Cholelithiasis, Colorectal Neoplasms, Crigler-Najjar syndrome, Diabetes Mellitus, Gastroschisis, Gaucher Disease, Gilbert Disease, Glycogen Storage Disease, Hepatocellular carcinoma, Hyperbilirubinemia, Leukopenia, Lucey-Driscoll syndrome, Malignant Neoplasm, Metabolic Syndrome, Neutropenia, Obesity, Prostate cancer, Stomach neoplasms, Thalassemia, Xeroderma Pigmentosum
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191330
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UDP glucuronosyltransferase family 1 member A6 |
GNT1, HLUGP, HLUGP1, UDPGT, UDPGT 1-6, UGT-1A, UGT-1C, UGT-1E, UGT-1F, UGT1, UGT1-01, UGT1-03, UGT1-05, UGT1-06, UGT1.1, UGT1.3, UGT1.5, UGT1.6, UGT1A, UGT1A1, UGT1A3, UGT1A5, UGT1A6S, UGT1C, UGT1E, UGT1F, hUG-BR1 |
Curated: Autism, Bilirubin metabolism disease, Cholecystolithiasis, Contact dermatitis, Crigler-najjar syndrome, Melanoma, Gallstones, Gilbert syndrome, Insomnia, Liver disease, Lucey-driscoll syndrome, Neuroblastoma, Nonalcoholic fatty liver disease, Perinatal disease
Unreviewed: Adenoma, alpha Thalassemia, Anemia, Asthma, Benign Prostatic Hyperplasia, beta Thalassemia, Bladder carcinoma, Bladder Neoplasm, Brain injuries, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoid tumor, Carcinoma, Cardiomyopathy, Cardiovascular disease, Cardiovascular Diseases, Cholelithiasis, Cholestasis, Colon Carcinoma, Colonic Neoplasms, Colorectal adenoma, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Coronary Arteriosclerosis, Crigler-Najjar syndrome, Deficiency Of Glucose-6-Phosphate Dehydrogenase, Dermatitis, Diabetes Mellitus, Diarrhea, Epilepsy, Gastritis, Gastrointestinal disease, Gastroschisis, Gaucher Disease, Gilbert Disease, Glycogen Storage Disease, Head and neck cancer, Head And Neck Carcinoma, Hepatitis c, Hereditary Spherocytosis, Hyperbilirubinemia, Kernicterus, Leukopenia, Liver failure, Liver neoplasms, Lucey-Driscoll syndrome, Lung Cancer, Lung carcinoma, Lung neoplasms, Lymphoblastic Leukemia, Malignant Neoplasm, Metabolic Syndrome, Myeloid Leukemia, Myocardial Ischemia, Neoplasms, Neutropenia, Non-Alcoholic Fatty Liver Disease, Obesity, Pancreatic neoplasm, Pancreatitis, Prostate cancer, Renal cell carcinoma, Rheumatoid arthritis, Seizures, Status Epilepticus, Stomach Carcinoma, Stomach Neoplasms, Thalassemia, Thyroid Carcinoma, Urinary bladder cancer, Urinary bladder neoplasms, Xeroderma Pigmentosum
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