|
241
|
|
|
Golgin B1 |
GCP, GCP372, GOLIM1 |
|
|
242
|
|
|
Glutamic-oxaloacetic transaminase 1 |
AST, AST1, ASTQTL1, GIG18, SGOT, cAspAT, cCAT |
|
|
243
|
|
|
Glutamic-oxaloacetic transaminase 2 |
DEE82, KAT4, KATIV, KYAT4, mitAAT |
|
|
244
|
|
|
Glycoprotein Ib platelet subunit alpha |
BDPLT1, BDPLT3, BSS, CD42B, CD42b-alpha, DBPLT3, GP1B, GPIbA, GPIbalpha, VWDP |
Alloimmune thrombocytopenia, Anemia, Asthma, Barber say syndrome, Bernard soulier syndrome, Brooke-spiegler syndrome, Cerebral palsy, Deficiency of platelet glycoprotein 1b, Developmental delay, Fetal and neonatal alloimmune thrombocytopenia, Hematomas, Hypertension, Macrothrombocytopenia, Migraine, Nonarteritic anterior ischemic optic neuropathy, Pseudo-von willebrand disease, Sensorineural hearing loss, Subarachnoid hemorrhage, Von willebrand disorderView all (4 more) |
|
245
|
|
|
Glycoprotein Ib platelet subunit beta |
BDPLT1, BS, CD42C, GPIBB, GPIbbeta |
22q11 deletion syndrome, 22q11 partial monosomy syndrome, 22q11.2 deletion syndrome, Acne, Acrocephaly, Alloimmune thrombocytopenia, Anxiety disorder, Arachnodactyly, Arrhinencephaly, Arthritis, Asthma, Asymmetric crying face association, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Barber say syndrome, Bernard soulier syndrome, Bipolar disorder, Bowel incontinence, Brooke-spiegler syndrome, Cataract, Cerebral palsy, 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, Deficiency of platelet glycoprotein 1b, Developmental delay, Digeorge syndrome, Dwarfism, Dysphasia, Fetal and neonatal alloimmune thrombocytopenia, Gastroesophageal reflux disease, Glaucoma, Hearing loss, Hematomas, Hirschsprung disease, Hydrocephalus, Hyperthyroidism, Hypoparathyroidism, Hypospadias, Hypothyroidism, Immunologic deficiency syndromes, Imperforate anus, Juvenile arthritis, Laryngomalacia, Macrothrombocytopenia, Major affective disorder, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Migraine, Multiple renal cysts, Myelomeningocele, Obesity, Optic atrophy, Otitis media, Sclerocystic ovaries, Patent ductus arteriosus, Persistent truncus arteriosus, Platybasia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Polycystic kidney disease, Polycystic ovary syndrome, Polydactyly of toes, Posterior embryotoxon, Ptosis, Renal hypoplasia, Schizophrenia, Scoliosis, Seborrheic dermatitis, Sensorineural hearing loss, Shprintzen syndrome, Specific learning disorder, Still disease, Strabismus, Subarachnoid hemorrhage, Tetralogy of fallot, Tricuspid atresia, Uterine anomalies, Ventricular septal defect, Vesicoureteral reflux, Vulval varicesView all (80 more) |
|
246
|
|
|
Glycoprotein 2 |
ZAP75 |
|
|
247
|
|
|
Glycoprotein IX platelet |
CD42a, GPIX |
|
|
248
|
|
|
Glypican 1 |
glypican |
|
|
249
|
|
|
Glycerol-3-phosphate dehydrogenase 1 |
GPD-C, GPDH-C, HTGTI |
|
|
250
|
|
|
Glycerol-3-phosphate dehydrogenase 2 |
GDH2, GPDM, mGDH, mGPDH |
|
