|
111
|
|
|
Ubiquitin C-terminal hydrolase L3 |
UCH-L3 |
|
|
112
|
|
|
Uroplakin 1B |
TSPAN20, UPIB, UPK1 |
|
|
113
|
|
|
Urocortin |
UCN1, UI, UROC |
|
|
114
|
|
|
Uncoupling protein 1 |
SLC25A7, UCP |
|
|
115
|
|
|
Uncoupling protein 2 |
BMIQ4, SLC25A8, UCPH |
Anaplastic carcinoma, Bipolar disorder, Carcinoma, Cerebral ischemia, Hyperinsulinemic hypoglycemia, Developmental delay, Diabetes mellitus, Fatty liver, Growth hormone deficiency, Hyperinsulinism, Hypertension, Hypoglycemia, Obesity, Schizophrenia, Stroke |
|
116
|
|
|
Uncoupling protein 3 |
SLC25A9 |
|
|
117
|
|
|
Ubiquitin recognition factor in ER associated degradation 1 |
UFD1L |
22q11 deletion syndrome, 22q11 partial monosomy syndrome, 22q11.2 deletion 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, Cataract, Choanal atresia, Cholelithiasis, Chronic obstructive pulmonary disease, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, 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, Imperforate anus, Laryngomalacia, Major affective disorder, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Multiple renal cysts, Myelomeningocele, Obesity, Optic atrophy, Otitis media, Patent ductus arteriosus, Persistent truncus arteriosus, Platybasia, Polycystic kidney disease, Polydactyly of toes, Posterior embryotoxon, Ptosis, Renal hypoplasia, Schizophrenia, Scoliosis, Seborrheic dermatitis, Shprintzen syndrome, Specific learning disorder, Strabismus, Tetralogy of fallot, Tricuspid atresia, Uterine anomalies, Ventricular septal defect, Vesicoureteral reflux, Vulval varicesView all (62 more) |
|
118
|
|
|
UDP-glucose ceramide glucosyltransferase |
GCS, GLCT1 |
|
|
119
|
|
|
UDP-glucose 6-dehydrogenase |
DEE84, EIEE84, GDH, UDP-GlcDH, UDPGDH, UGD |
|
|
120
|
|
|
UDP-glucose pyrophosphorylase 2 |
DEE83, EIEE83, SVUGP2, UDPG, UDPGP, UDPGP2, UGP1, UGPP1, UGPP2, pHC379 |
|
