|
321
|
|
|
Glutathione S-transferase pi 1 |
DFN7, FAEES3, GST3, GSTP, HEL-S-22, PI |
Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Anaplastic carcinoma, Asthma, Autism, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Carotid artery disease, Carotid atherosclerosis, Chromophobe carcinoma, Classical hodgkin lymphoma, Coronary syndrome, Dermatitis, Gastric cancer, Glioma, Hodgkin disease, Hodgkin lymphoma, Hodgkin lymphoma, lymphocyte depletion, Hypertension, Kidney disease, Kidney failure, Kidney stone, Liver carcinoma, Lung carcinoma, Lung neoplasms, Lung cancer, Marfan syndrome, Moyamoya disease, Myeloid leukemia, Myocardial ischemia, Nervous system diseases, Non-alcoholic fatty liver disease, Nonorganic psychosis, Osteosarcoma, Papillary renal carcinoma, Parkinson disease, Prostatic neoplasms, Prostate cancer, Psychosis, Renal carcinoma, Acute kidney insufficiency, Sarcoma, Schizophrenia, Shared paranoid disorder, Stomach neoplasms, Tremor, Ureteral calculi, Vestibular diseasesView all (37 more) |
|
322
|
|
|
Glutathione S-transferase theta 1 |
- |
Anaplastic carcinoma, Asbestosis, Asthenozoospermia, Benign neoplasm, Bipolar disorder, Carcinoma, Chromophobe carcinoma, Esophagus neoplasm, Giant cell glioblastoma, Glioblastoma, Hypertension, Kidney neoplasm, Kidney cancer, Lung neoplasms, Lung cancer, Malignant neoplasm, Mental depression, Multiple myeloma, Neoplasms, Non-alcoholic fatty liver disease, Papillary renal carcinoma, Prostatic neoplasms, Prostate cancer, Raynaud disease, Raynaud phenomenon, Renal carcinoma, Schizophrenia, Skin cancer, Skin neoplasmsView all (14 more) |
|
323
|
|
|
Glutathione S-transferase theta 2 (gene/pseudogene) |
- |
|
|
324
|
|
|
Glutathione S-transferase zeta 1 |
GSTZ1-1, MAAI, MAAID, MAI |
|
|
325
|
|
|
General transcription factor IIA subunit 1 |
TF2A1, TFIIA, TFIIA-42, TFIIAL |
|
|
326
|
|
|
General transcription factor IIB |
TF2B, TFIIB |
|
|
327
|
|
|
General transcription factor IIE subunit 2 |
FE, TF2E2, TFIIE-B, TTD6 |
Anemia, Astigmatism, Bronchospasm, Carcinoma, Cardiomyopathy, Cerebral cortical atrophy, Congenital epicanthus, Congenital exfoliative erythroderma, Congenital exomphalos, Coronal craniosynostosis, Craniosynostosis, Cryptorchidism, Dental enamel hypoplasia, Developmental delay, Dwarfism, Dysarthria, Ectropion, Eczema, Esotropia, Gonadal dysgenesis, Hypoplasia of mandible relative to maxilla, Ichthyosis, Impaired social reciprocity, Keratoconjunctivitis sicca, Age-related macular degeneration, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Motor delay, Myopia, Nervous system diseases, Neutropenia, Nystagmus, Osteopenia, Osteosclerosis, Paraplegia, Partial agenesis of corpus callosum, Periventricular leukomalacia, Seizure, Sensorineural hearing loss, Trichothiodystrophy, Ventricular septal defectView all (28 more) |
|
328
|
|
|
General transcription factor IIH subunit 4 |
P52, TFB2, TFIIH |
|
|
329
|
|
|
General transcription factor IIi |
BAP135, BTKAP1, DIWS, GTFII-I, IB291, SPIN, TFII-I, WBS, WBSCR6 |
Abnormal dermatoglyphic pattern, Abnormal spinal segmentation, Accessory kidney, Aneurysm of aortic arch, Anxiety disorder, Arnold-chiari malformation, Atrial fibrillation, Atrial septal defect, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Bicuspid aortic valve, Bladder diverticulum, Blepharophimosis, Camptodactyly of fingers, Cardiovascular diseases, Cataract, Cerebral cortical atrophy, Cholelithiasis, Chronic obstructive pulmonary disease, Congenital anomaly of neck, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital pectus excavatum, Congestive heart failure, Cornea plana, Cryptorchidism, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dysgraphia, Gastroesophageal reflux disease, Glaucoma, Hearing loss, Hypercalcemia, Hypertension, Hypertrophic cardiomyopathy, Hypodontia, Hypogonadotropic hypogonadism, Hypothyroidism, Leukemia, Macroglossia, Macrostomia, Macrotia, Malabsorption syndrome, Mental depression, Mental retardation, Microcephaly, Microdontia, Micrognathism, Mitral valve prolapse, Multiple renal cysts, Myeloid leukemia, Myocardial infarction, Myopathy, Myopia, Nephrocalcinosis, Nephrolithiasis, Nystagmus-induced head nodding, Obesity, Obsessive-compulsive disorder, Osteopenia, Osteoporosis, Osteosclerosis, Otitis media, Overriding aorta, Paroxysmal atrial fibrillation, Patent ductus arteriosus, Pelvic kidney, Peptic ulcer, Peripheral pulmonary artery stenosis, Phakomatosis pigmentovascularis, Polycystic ovary syndrome, Posterior embryotoxon, Precocious puberty, Pulmonary stenosis, Radioulnar synostosis, Rectal prolapse, Renal hypoplasia, Renal insufficiency, Scoliosis, Sjogren`s syndrome, Spina bifida occulta, Strabismus, Stroke, Supravalvar aortic stenosis, Tetralogy of fallot, Thymic tumor, Ventricular septal defect, Vesicoureteral reflux, Williams syndromeView all (79 more) |
|
330
|
|
|
- |
- |
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