Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14421 to 14430 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14421
Ubiquitin-fold modifier conjugating enzyme 1
HSPC155, NEDSG
Alzheimer disease, Neurodevelopmental disorder

14422
Ubiquitin recognition factor in ER associated degradation 1
UFD1L
22q11.2 deletion syndrome, Congenital heart disease, Craniofacial abnormalities, Digeorge syndrome, Congenital heart defect, Schizophrenia

14423
UFM1 specific ligase 1
KIAA0776, Maxer, NLBP, RCAD
Migraine

14424
Ubiquitin fold modifier 1
BM-002, C13orf20, HLD14
Central nervous system cancer, Long qt syndrome, Glioblastoma, Glioma, Hypomyelinating leukodystrophy

14425
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

14426
UDP-glucose ceramide glucosyltransferase
GCS, GLCT1
Benign prostatic hyperplasia, Congenital nonbullous ichthyosiform erythroderma, Hypertension, Ichthyosis, Liver cirrhosis, Myocardial ischemia

14427
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

14428
UDP-glucose glycoprotein glucosyltransferase 1
HUGT1, UGCGL1, UGT1
Color vision deficiency, Disorder of protein n-glycosylation

14429
UDP-glucose glycoprotein glucosyltransferase 2
HUGT2, UGCGL2, UGT2
Gout, Schizophrenia, Vascular disease

14430
UDP-glucose pyrophosphorylase 2
DEE83, EIEE83, SVUGP2, UDPG, UDPGP, UDPGP2, UGP1, UGPP1, UGPP2, pHC379
Developmental and epileptic encephalopathy, Insomnia