Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14361 to 14370 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14361
Ubiquitin fold modifier 1
BM-002, C13orf20, HLD14
Central nervous system cancer, Long qt syndrome, Glioblastoma, Glioma, Hypomyelinating leukodystrophy

14362
UFM1 specific peptidase 2
BHD, C4orf20, DEE106, SEMDDR
Nonsyndromic intellectual disability, Beukes hip dysplasia, Color vision deficiency, Congenital hip dysplasia, Congenital neurologic anomalies, Desbuquois syndrome, Developmental and epileptic encephalopathy, Intellectual developmental disorder, Seizures, Spondyloepimetaphyseal dysplasia, Systemic sclerosis

14363
UDP-glucose ceramide glucosyltransferase
GCS, GLCT1
Benign prostatic hyperplasia, Congenital nonbullous ichthyosiform erythroderma, Hypertension, Ichthyosis, Myocardial ischemia

14364
UDP-glucose 6-dehydrogenase
DEE84, EIEE84, GDH, UDP-GlcDH, UDPGDH, UGD
Cholecystolithiasis, Color vision deficiency, Congenital heart disease, Developmental and epileptic encephalopathy, Gallstones, Hemorrhoid, Liver neoplasms, Peripheral arterial disease, West syndrome

14365
UDP-glucose glycoprotein glucosyltransferase 1
HUGT1, UGCGL1, UGT1
Color vision deficiency, Congenital disorder of glycosylation

14366
UDP-glucose glycoprotein glucosyltransferase 2
HUGT2, UGCGL2, UGT2
Gout, Schizophrenia, Vascular disease

14367
UDP-glucose pyrophosphorylase 2
DEE83, EIEE83, SVUGP2, UDPG, UDPGP, UDPGP2, UGP1, UGPP1, UGPP2, pHC379
Developmental and epileptic encephalopathy, Insomnia

14368
UDP glucuronosyltransferase family 1 member A1
BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT 1-1, UGT1, UGT1A
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
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14369
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
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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14370
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