Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
14311 to 14320 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14311
UBE2V1 pseudogene 16
-
Orofacial cleft, Scoliosis, Thoracic aortic aneurysm

14312
Ubiquitin conjugating enzyme E2 V2
DDVIT1, DDVit-1, EDAF-1, EDPF-1, EDPF1, MMS2, UEV-2, UEV2
Alzheimer disease, Attention deficit hyperactivity disorder, Corneal ulcer, Crohn disease, Eye disease, Inflammatory bowel disease, Ulcerative colitis

14313
Ubiquitin conjugating enzyme E2 W
UBC-16, UBC16
Alzheimer disease, Color vision deficiency, Dementia, Insomnia, Metabolic syndrome, Osteoarthritis, Diabetes mellitus type 2

14314
Ubiquitin conjugating enzyme E2 Z
HOYS7, USE1
Coronary artery disease, Insomnia, Myocardial infarction, Prostate cancer, Schizophrenia, Diabetes mellitus type 2

14315
Ubiquitin protein ligase E3A
ANCR, AS, E6-AP, EPVE6AP, HPVE6A, PIX1
15q11q13 microduplication syndrome, Angelman syndrome, Autism, Craniofacial abnormalities, Developmental delay, Developmental disability, Duplication 15q11-q13 syndrome, Epilepsy, Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder, Obesity, Prostate cancer

14316
Ubiquitin protein ligase E3B
BPIDS, KOS
Blepharophimosis intellectual disability syndrome, Coronary artery disease, Insomnia, Major depressive disorder, Neurotic disorder, Oculocerebrofacial syndrome, Polymyositis, Schizophrenia

14317
Ubiquitin protein ligase E3C
HECTH2, NDSMBA, NEDSMBA, RAUL
Juvenile arthritis, Dementia, Diabetes mellitus, Diabetic neuropathy, Diabetic retinopathy, Juvenile idiopathic arthritis, Language development disorders, Metabolic syndrome, Neurodevelopmental disorder, Oligoarticular juvenile idiopathic arthritis, Squamous cell carcinoma, Diabetes mellitus type 2

14318
Ubiquitin protein ligase E3D
C6orf157, H10BH, UBE2CBP, YJR141W
Bipolar disorder, Color vision deficiency, Crohn disease, Dry eye syndrome, Esophageal squamous cell carcinoma, Inflammatory bowel disease, Major depressive disorder, Metabolic syndrome, Pelvic organ prolapse, Schizophrenia, Scoliosis, Diabetes mellitus type 2

14319
Ubiquitination factor E4A
E4, NEDHMS, UBOX2, UFD2
Nonsyndromic intellectual disability, Lung cancer, Major depressive disorder, Neurodevelopmental disorder

14320
Ubiquitination factor E4B
E4, HDNB1, UBOX3, UFD2, UFD2A
1p36 deletion syndrome, Alzheimer disease, Atrial fibrillation, Atrial flutter, Brain injuries, Chromosome 1p36 deletion syndrome, Developmental disability, Wallerian degeneration