|
51
|
|
|
UTP20 small subunit processome component |
1A6/DRIM, DRIM |
|
|
52
|
|
|
Urotensin 2 receptor |
GPR14, UR-2-R, UTR, UTR2 |
|
|
53
|
|
|
Unc-80 subunit of NALCN channel complex |
C2orf21, UNC-80 |
Apnea, Autism spectrum disorder, Brachycephaly, Camptodactyly of fingers, Congenital epicanthus, Developmental delay, Eczema, Encephalopathy, Esotropia, Frontal bossing, High palate, Hyperopic astigmatism, Hypoplasia of corpus callosum, Hypotonia, with psychomotor retardation and characteristic facies, Hypotonia, speech impairment, severe cognitive delay syndrome, Hypotonia-speech impairment-severe cognitive delay syndrome, Mental retardation, Laryngomalacia, Microcephaly, Micrognathism, Nystagmus, Osteopenia, Plagiocephaly, Posteriorly rotated ear, Ptosis, Respiratory failure, Sleep apnea, StrabismusView all (13 more) |
|
54
|
|
|
Ubiquitin conjugating enzyme E2 T |
FANCT, HSPC150, PIG50 |
Anemia, Astigmatism, Atrial septal defect, Azoospermia, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Fanconi anemia, Frontal bossing, High palate, Hirschsprung disease, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypoplasia of thumb, Hypospadias, Imperforate anus, Kidney neoplasm, Kidney cancer, Leukemia, Leukopenia, Liver carcinoma, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Nystagmus, Pancytopenia, Patent ductus arteriosus, Proptosis, Ptosis, Renal insufficiency, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallotView all (37 more) |
|
55
|
|
|
Ubiquitin like with PHD and ring finger domains 1 |
ICBP90, Np95, RNF106, TDRD22, hNP95, hUHRF1, huNp95 |
|
|
56
|
|
|
Ubiquinol-cytochrome c reductase, complex III subunit X |
HSPC051, HSPC119, HSPC151, QCR9, UCCR7.2, UCRC |
|
|
57
|
|
|
Ubinuclein 1 |
VT, VT4 |
|
|
58
|
|
|
UbiA prenyltransferase domain containing 1 |
SCCD, TERE1 |
|
|
59
|
|
|
Ubiquilin 2 |
ALS15, CHAP1, DSK2, HRIHFB2157, N4BP4, PLIC2 |
Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis, with or without frontotemporal dementia, Anxiety disorder, Dysarthria, Dysphagia, Frontotemporal dementia, Laryngospasm, Mental depression, Mood swings, Respiratory failure |
|
60
|
|
|
UBA domain containing 2 |
PHGDHL1 |
Acne, Anorexia, Aortic valve insufficiency, Aphthous ulcer, Arthritis, Asthma, Basal cell neoplasm, Behcet syndrome, Carcinoma, Cataract, Cranial nerve paralysis, Crohn disease, Developmental regression, Encephalitis, Endocarditis, Gangrene, Inflammatory bowel disease, Keratoconjunctivitis sicca, Malabsorption syndrome, Migraine, Myocardial infarction, Myositis, Oral ulcer, Pancreatitis, Pericarditis, Pleural effusion, Pleuritis, Psoriasis, Renal glomerular disease, Renal insufficiency, Respiratory tract diseases, Retinal diseases, Retrobulbar neuritis, Ulcerative colitis, Vascular diseases, VasculitisView all (21 more) |
