Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "U"

101 to 110 of 268 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
101	23376	UFL1	UFM1 specific ligase 1	KIAA0776, Maxer, NLBP, RCAD	Migraine
102	51569	UFM1	Ubiquitin fold modifier 1	BM-002, C13orf20, HLD14	Central nervous system cancer, Long qt syndrome, Glioblastoma, Glioma, Hypomyelinating leukodystrophy
103	55325	UFSP2	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
104	7357	UGCG	UDP-glucose ceramide glucosyltransferase	GCS, GLCT1	Benign prostatic hyperplasia, Congenital nonbullous ichthyosiform erythroderma, Hypertension, Ichthyosis, Liver cirrhosis, Myocardial ischemia
105	7358	UGDH	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
106	56886	UGGT1	UDP-glucose glycoprotein glucosyltransferase 1	HUGT1, UGCGL1, UGT1	Color vision deficiency, Disorder of protein n-glycosylation
107	55757	UGGT2	UDP-glucose glycoprotein glucosyltransferase 2	HUGT2, UGCGL2, UGT2	Gout, Schizophrenia, Vascular disease
108	7360	UGP2	UDP-glucose pyrophosphorylase 2	DEE83, EIEE83, SVUGP2, UDPG, UDPGP, UDPGP2, UGP1, UGPP1, UGPP2, pHC379	Developmental and epileptic encephalopathy, Insomnia
109	54658	UGT1A1	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, Hepatitis b, Hodgkin disease, Hyperbilirubinemia, Insomnia, Kidney failure View all (4 more)
110	54575	UGT1A10	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, Urinary bladder cancer View all (1 more)

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