Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "U"
111 to 120 of 268 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

111
UDP glucuronosyltransferase family 1 member A3
UDPGT, UDPGT 1-3, UGT-1C, UGT1-03, UGT1.3, UGT1A3S, UGT1C
Bilirubin metabolism disease, Cholecystolithiasis, Crigler-najjar syndrome, Gallstones, Gilbert syndrome, Insomnia, Liver disease, Lucey-driscoll syndrome, Nonalcoholic fatty liver disease, Perinatal disease, Schizophrenia

112
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
Bilirubin metabolism disease, Celiac disease, Cholecystolithiasis, Crigler-najjar syndrome, Gallstones, Gilbert syndrome, Insomnia, Liver disease, Lucey-driscoll syndrome, Nonalcoholic fatty liver disease, Perinatal disease

113
UDP glucuronosyltransferase family 1 member A5
UDPGT, UDPGT 1-5, UGT1E
Bilirubin metabolism disease, Cholecystolithiasis, Crigler-najjar syndrome, Gallstones, Gilbert syndrome, Insomnia, Liver disease, Lucey-driscoll syndrome, Nonalcoholic fatty liver disease, Perinatal disease

114
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
Autism, Bilirubin metabolism disease, Cholecystolithiasis, Contact dermatitis, Crigler-najjar syndrome, Melanoma, Gallstones, Gilbert syndrome, Hepatitis b, Insomnia, Liver disease, Lucey-driscoll syndrome, Neuroblastoma, Nonalcoholic fatty liver disease, Perinatal disease

115
UDP glucuronosyltransferase family 1 member A7
GNT1, UDPGT, UDPGT 1-7, UGT-1A, UGT-1G, UGT1, UGT1-01, UGT1-07, UGT1.1, UGT1.7, UGT1A, UGT1A1, UGT1G, hUG-BR1
Bilirubin metabolism disease, Cholecystolithiasis, Crigler-najjar syndrome, Melanoma, Gallstones, Gilbert syndrome, Insomnia, Liver disease, Lucey-driscoll syndrome, Neuroblastoma, Nonalcoholic fatty liver disease, Pancreatitis, Perinatal disease

116
UDP glucuronosyltransferase family 1 member A8
GNT1, UDPGT, UDPGT 1-1, UDPGT 1-8, UGT-1A, UGT-1H, UGT1, UGT1-01, UGT1-08, UGT1.1, UGT1.8, UGT1A, UGT1A1, UGT1A8S, UGT1H, hUG-BR1
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
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117
UDP glucuronosyltransferase family 1 member A9
HLUGP4, LUGP4, UDPGT, UDPGT 1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1A9S, UGT1AI, UGT1I
Attention deficit hyperactivity disorder, Bilirubin metabolism disease, Cholecystolithiasis, Crigler-najjar syndrome, Melanoma, Gallstones, Gilbert syndrome, Insomnia, Kidney failure, Liver disease, Lucey-driscoll syndrome, Neuroblastoma, Nonalcoholic fatty liver disease, Perinatal disease

118
UDP glucuronosyltransferase family 2 member A1 complex locus
UDPGT2A1
Autism, Ovarian epithelial cancer, Ovarian cancer, Hypertension, Uterine fibroid

119
UDP glucuronosyltransferase family 2 member A2
UDPGT 2A2
Ovarian epithelial cancer, Ovarian cancer

120
UDP glucuronosyltransferase family 2 member A3
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Autism