|
101
|
|
|
Ubiquitin like modifier activating enzyme 7 |
D8, UBA1B, UBE1L, UBE2, UBE7 |
|
|
102
|
|
|
Ubiquitin conjugating enzyme E2 A |
HHR6A, MRXS30, MRXSN, RAD6A, UBC2 |
Cryptorchidism, Developmental delay, Double outlet right ventricle, Dysmorphic features, Hyperbilirubinemia, Hypospadias, Mental retardation, Macrocephaly, Macrostomia, Macrotia, Mental retardation, x-linked, Mitral valve stenosis, Nail diseases, Nail dysplasia, Nail dystrophy, Neutropenia, Obsessive-compulsive disorder, Patchy hypo- and hyperpigmentation, Patent ductus arteriosus, Patent foramen ovale, Penis agenesis, Peripheral pulmonary artery stenosis, Pulmonary arterial hypertension, Strabismus, Synophrys, Tetralogy of fallot, Ventricular septal defect, Vesicoureteral refluxView all (13 more) |
|
103
|
|
|
Ubiquitin conjugating enzyme E2 E1 |
UBCH6 |
|
|
104
|
|
|
Ubiquitin conjugating enzyme E2 E2 |
UBCH8 |
|
|
105
|
|
|
Ubiquitin conjugating enzyme E2 H |
E2-20K, GID3, UBC8, UBCH, UBCH2 |
|
|
106
|
|
|
Ubiquitin conjugating enzyme E2 I |
C358B7.1, P18, UBC9 |
|
|
107
|
|
|
Ubiquitin conjugating enzyme E2 L3 |
E2-F1, L-UBC, UBCH7, UbcM4 |
Alzheimer disease, Ankylosing spondylitis, Arthritis, Autoimmune diseases, Cholangitis, Crohn disease, Immune system diseases, Inflammatory bowel disease, Lupus erythematosus, Oligoarticular arthritis, Pauciarticular chronic arthritis, Seronegative polyarthritis, Psoriasis, Psoriasis vulgaris, Rheumatoid arthritis, Still disease, Systemic lupus erythematosus, Ulcerative colitisView all (3 more) |
|
108
|
|
|
Ubiquitin protein ligase E3A |
ANCR, AS, E6-AP, EPVE6AP, HPVE6A, PIX1 |
15q11q13 microduplication syndrome, Angelman syndrome, Apraxia, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Camptodactyly of fingers, Cerebral cortical atrophy, Congenital epicanthus, Developmental delay, Dwarfism, Dysmorphic features, Epilepsy, Exotropia, Hypopigmentation disorder, Hypoplasia of the maxilla, Mental retardation, Macrocephaly, Macroglossia, Macrostomia, Malocclusion, Motor delay, Movement disorders, Myopia, Nystagmus, Obesity, Obsessive-compulsive disorder, Scoliosis, Strabismus, Syndactyly of fingersView all (15 more) |
|
109
|
|
|
Upstream binding transcription factor |
CONDBA, NOR-90, UBF, UBF-1, UBF1, UBF2 |
Autism, Cerebellar atrophy, Cerebral cortical atrophy, Developmental delay, Developmental regression, Dysphagia, Dysphasia, Hypoplasia of corpus callosum, Motor and cognitive regression syndrome with extrapyramidal movement disorder, Neurodegenerative disorders with brain atrophy, Parkinson disease |
|
110
|
|
|
Ubiquitin C-terminal hydrolase L1 |
HEL-117, HEL-S-53, NDGOA, PARK5, PGP 9.5, PGP9.5, PGP95, SPG79, SPG79A, UCHL-1, Uch-L1 |
Abnormal male sexual function, Anxiety disorder, Cerebellar atrophy, Cerebral atrophy, Dementia of frontal lobe, Dysautonomia, Dyskinetic syndrome, Esophagus neoplasm, Female sexual dysfunction, Neoplasm of gallbladder, Gallbladder cancer, Gastroparesis, Hallucinations, Liver carcinoma, Lung carcinoma, Male sexual dysfunction, Mental depression, Myopia, Nervous system diseases, Neurodegeneration-blindness-ataxia-spasticity syndrome, Nystagmus, Optic atrophy, Panic disorder, Parkinson disease, Restless legs syndrome, Sensorimotor neuropathy, Social communication disorder, Spastic paraplegiaView all (13 more) |
