191301
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Ubiquitin-fold modifier conjugating enzyme 1 |
HSPC155, NEDSG |
Curated: Alzheimer disease, Neurodevelopmental disorder
Unreviewed: Arthritis, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Developmental and epileptic encephalopathy, Developmental disability, Dwarfism, Liver Cancer, Liver carcinoma, Malignant Neoplasm, Mental retardation, Microcephaly, Neoplasms, Neurodevelopmental Disorder With Spasticity And Poor Growth, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Stomach Carcinoma, Stomach Neoplasms, Stroke
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191302
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UFC1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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191303
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Ubiquitin recognition factor in ER associated degradation 1 |
UFD1L |
Curated: 22q11.2 deletion syndrome, Congenital heart disease, Craniofacial abnormalities, Digeorge syndrome, Congenital heart defects, Schizophrenia
Unreviewed: 22q11 deletion syndrome, 22q11 partial monosomy syndrome, Acne, Acrocephaly, Anxiety Disorder, Arachnodactyly, Arrhinencephaly, Arthritis, Asthma, Asymmetric crying face association, Atrial Septal Defect, Attention Deficit Hyperactivity Disorder, Autism, Bipolar Disorder, Bowel incontinence, Carcinoma, Cataract, Choanal Atresia, Cholelithiasis, Chronic Obstructive Pulmonary Disease, Cognitive disorder, Colon Carcinoma, Colonic Neoplasms, Congenital Clubfoot, Congenital Epicanthus, Congenital Exomphalos, Congenital Hypoplasia Of Thymus, Congenital malrotation of intestine, Conotruncal Anomaly Face Syndrome, Corneal Neovascularization, Cryptorchidism, Developmental Delay, DiGeorge Syndrome, Dwarfism, Dysphasia, Gastroesophageal Reflux Disease, Glaucoma, Hearing Loss, Hirschsprung Disease, Hydrocephalus, Hyperthyroidism, Hypoparathyroidism, Hypospadias, Hypothyroidism, Immunologic Deficiency Syndromes, Impaired Cognition, Imperforate anus, Laryngomalacia, Leukemia, Lymphoblastic Leukemia, Major Affective Disorder, Mental Depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Multiple renal cysts, Myelomeningocele, Myxopapillary Ependymoma, Obesity, Optic Atrophy, Otitis media, Patent ductus arteriosus, Persistent truncus arteriosus, Platybasia, Polycystic kidney disease, Polydactyly Of Toes, Posterior embryotoxon, Ptosis, Renal hypoplasia, Scoliosis, Seborrheic dermatitis, Shprintzen Syndrome, Shprintzen-Goldberg Syndrome, Specific Learning Disorder, Strabismus, Testicular regression syndrome, Tetralogy of Fallot, Tricuspid Atresia, Uterine Anomalies, Ventricular septal defect, Vesicoureteral Reflux, Vulval varices
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191304
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UFD1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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191305
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UFD1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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191306
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UFM1 specific ligase 1 |
KIAA0776, Maxer, NLBP, RCAD |
Curated: Migraine
Unreviewed: Adenocarcinoma, Breast neoplasm, Carcinogenesis, Cardiomyopathy, Congestive Heart Failure, Heart Failure, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Neoplasms, Ovarian diseases, Ovarian neoplasm, Renal Insufficiency
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191307
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UFL1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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191308
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Ubiquitin fold modifier 1 |
BM-002, C13orf20, HLD14 |
Curated: Central nervous system cancer, Long qt syndrome, Glioblastoma, Glioma, Hypomyelinating leukodystrophy, leukodystrophy, hypomyelinating, 14
Unreviewed: Anodontia, Arteriosclerosis, Atherosclerosis, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiomyopathy, Cerebellar atrophy, Cerebral Atrophy, Congestive Heart Failure, Demyelinating diseases, Developmental disability, Diabetes, Diabetes Mellitus, Epileptic encephalopathy, Gastritis, Heart Failure, Hip Dysplasia, Hypomyelinating Leukodystrophy, Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum, Mental retardation, Metachromatic leukodystrophy, Microcephaly, Neoplasms, Nervous System Disorder, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Triple negative breast cancer
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191309
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UFM1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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191310
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UFM1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
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