71
|
|
|
Beta-ureidopropionase 1 |
BUP1 |
Autism, Beta-ureidopropionase deficiency, Bladder exstrophy, Celiac disease, Cryptogenic west syndrome, Developmental delay, Jackknife seizures, Metabolic diseases, Hypotonia, Salaam seizures, Spasmus nutans, Speech disorders, Symptomatic west syndrome, West syndrome |
72
|
|
|
Ubiquitin associated and SH3 domain containing A |
CLIP4, STS-2, TULA, TULA-1 |
Ankylosing spondylitis, Autoimmune diseases, Celiac disease, Cholangitis, Crohn disease, Diabetes mellitus, Hypothyroidism, Immune system diseases, Multiple sclerosis, Psoriasis, Rheumatoid arthritis, Sclerosing cholangitis, Ulcerative colitis, Vitiligo |
73
|
|
|
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 |
|
74
|
|
|
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 |
|
75
|
|
|
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 |
|
76
|
|
|
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 |
|
77
|
|
|
UDP glucuronosyltransferase family 1 member A5 |
UDPGT, UDPGT 1-5, UGT1E |
|
78
|
|
|
UDP glucuronosyltransferase family 1 member A9 |
HLUGP4, LUGP4, UDPGT, UDPGT 1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1A9S, UGT1AI, UGT1I |
|
79
|
|
|
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 |
|
80
|
|
|
UDP glucuronosyltransferase family 1 member A1 |
BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT 1-1, UGT1, UGT1A |
Cerebral palsy, Classical hodgkin lymphoma, Crigler-najjar syndrome, Dermatitis, Epileptic encephalopathy, Gilbert disease, Hodgkin disease, Hodgkin lymphoma, Hodgkin lymphoma, lymphocyte depletion, Hyperbilirubinemia, Kernicterus, Kidney failure, Lucey-driscoll syndrome, Malignant neoplasm, Mental retardation, Metabolic syndrome, Neutropenia, Obesity, Oculomotor nerve palsy, Acute kidney insufficiency, Transient hyperbilirubinemiaView all (6 more) |