Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14381 to 14390 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14381
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

14382
Ubiquitination factor E4A
E4, NEDHMS, UBOX2, UFD2
Nonsyndromic intellectual disability, Lung cancer, Major depressive disorder, Neurodevelopmental disorder

14383
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

14384
UbiA prenyltransferase domain containing 1
SCCD, TERE1
Connective tissue disease, Corneal dystrophy, Edema, Intracranial hemorrhage

14385
Ubiquitin like 3
HCG-1, PNSC1
Breast cancer

14386
Ubiquitin like domain containing CTD phosphatase 1
CPUB1
Eczema, Autoimmune disease, Breast neoplasms, Inflammatory skin disease, Psoriasis, Schizophrenia, Systemic lupus erythematosus

14387
Ubinuclein 1
VT, VT4
Cardiovascular disease, Coronary artery disease, Non-immune hydrops fetalis, Metabolic syndrome, Diabetes mellitus type 2

14388
Ubinuclein 2
-
Autism, Central nervous system cancer, Glioblastoma, Glioma

14389
Ubiquilin 1
DA41, DSK2, PLIC-1, UBQN, XDRP1
Colorectal cancer, Intellectual developmental disorder

14390
Ubiquilin 2
ALS15, CHAP1, DSK2, HRIHFB2157, N4BP4, PLIC2
Amyotrophic lateral sclerosis, Androgenetic alopecia, Vascular dementia, Hypogonadism, Neurotic disorder