|
3671
|
|
|
Rho GTPase activating protein 45 |
HA-1, HLA-HA1, HMHA1 |
|
|
3672
|
|
|
Zinc finger protein 281 |
GZP1, ZBP-99, ZBP99, ZNP-99 |
|
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3673
|
|
|
Cardiotrophin like cytokine factor 1 |
BSF-3, BSF3, CISS2, CLC, NNT-1, NNT1, NR6 |
Cubitus valgus, Clinodactyly, Cold-induced sweating syndrome, Crisponi syndrome, Facial paralysis, High palate, Hypohidrosis, Impaired cognition, Micrognathism, Microstomia, Scoliosis, Sensorimotor neuropathy, Syndactyly of the toes, Thoracolumbar scoliosis |
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3674
|
|
|
Fos proto-oncogene, AP-1 transcription factor subunit |
AP-1, C-FOS, p55 |
Acanthosis nigricans, Amyotrophic lateral sclerosis, Anxiety disorder, Arthritis, Atherosclerosis, Atrial fibrillation, Breast cancer, Breast carcinoma, Cerebral infraction, Cerebral thrombosis, Cholestasis, Cirrhosis, Clonic seizures, Congenital lipodystrophy, Congestive heart failure, Diabetes mellitus, Endometrioma, Endometriosis, Epilepsy, Fatty liver, Fibrocartilaginous dysplasia of bone, Fibrocystic dysplasia of bone, Fibrous dysplasia, Grand mal status epilepticus, Hyperinsulinism, Hypertension, Hypertrophic cardiomyopathy, Hypotonic seizures, Immunologic deficiency syndromes, Isolated somatotropin deficiency, Jacksonian seizure, Juvenile arthritis, Kidney disease, Lateral sclerosis, Lipoatrophic diabetes mellitus, Lipoatrophy, Lipodystrophy, Liver carcinoma, Liver failure, Lung cancer, Lung neoplasms, Malocclusion, Mammary neoplasms, Marfan syndrome, Mental retardation, Myocardial infarction, Myopathy, Nervous system diseases, Nervous system disorder, Nonconvulsive status epilepticus, Osteopenia, Osteoporosis, Ovarian epithelial carcinoma, Pancreatitis, Petit mal status, Polyarthritis, rheumatoid factor positive, Polycystic ovary syndrome, Precocious puberty, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Scoliosis, Secondary physiologic amenorrhea, Seizure, Seronegative polyarthritis, Somatotropin deficiency, Status epilepticus, Still disease, Talipes transversoplanus, Trigeminal neuralgia, Ventricular hypertrophyView all (56 more) |
|
3675
|
|
|
Nicotinamide nucleotide transhydrogenase |
GCCD4 |
Adrenal hypoplasia, x-linked, Anorexia, Azoospermia, Chronic obstructive pulmonary disease, Congenital hypothyroidism, Cryptorchidism, Glucocorticoid deficiency, Glucocorticoid deficiency with or without mineralocorticoid deficiency, Glucocorticoid deficiency with mineralocorticoid deficiency, Hypernatriuria, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoglycemic coma, Hypoglycemic seizures, Mental retardation, Precocious puberty, Quadriplegia, Testicular adrenal rest tumorView all (3 more) |
|
3676
|
|
|
PRAME nuclear receptor transcriptional regulator |
CT130, MAPE, OIP-4, OIP4 |
Chromophobe carcinoma, Head and neck neoplasms, Head neoplasms, Neck cancer, Neoplasm of head, Leukemia, Lung carcinoma, Head and neck cancer, Medulloblastoma, Medullomyoblastoma, Melanoma, Multiple myeloma, Myeloid leukemia, Neck neoplasms, Papillary renal carcinoma, Renal carcinoma, Sarcoma, Upper aerodigestive tract neoplasmsView all (3 more) |
|
3677
|
|
|
Phosphoinositide-3-kinase regulatory subunit 5 |
F730038I15Rik, FOAP-2, P101-PI3K, p101 |
Ataxia-oculomotor apraxia, Cerebellar atrophy, Choreoathetosis, Colorectal cancer, Dysarthria, Dysphagia, Hypercholesterolemia, Hypoalbuminemia, Hypothyroidism, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Polyneuropathy, Sensorimotor neuropathy, Spinocerebellar ataxia, Spinocerebellar ataxia, with axonal neuropathy, StrabismusView all (2 more) |
|
3678
|
|
|
Transportin 3 |
IPO12, LGMD1F, LGMDD2, MTR10A, TRN-SR, TRN-SR2, TRNSR |
Biliary cholangitis, Biliary cirrhosis, Celiac disease, Cirrhosis, Conjugated hyperbilirubinemia, Dermatographic urticaria, Gastrointestinal inflammation, Hypoalbuminemia, Limb-girdle muscular dystrophy, Liver carcinoma, Liver failure, Liver fibrosis, Lupus erythematosus, Muscular dystrophy, Myositis, Osteoporosis, Portal hypertension, Rheumatoid arthritis, Scleroderma, Sjogren`s syndromeView all (5 more) |
|
3679
|
|
|
Solute carrier family 16 member 8 |
MCT3, REMP |
|
|
3680
|
|
|
FosB proto-oncogene, AP-1 transcription factor subunit |
AP-1, G0S3, GOS3, GOSB |
Arthritis, Cognitive disorder, Dyskinesia, Epilepsy, Impulse control disorder, Intermittent explosive disorder, Juvenile arthritis, Liver neoplasms, Liver cancer, Liver carcinoma, Lung neoplasms, Lung cancer, Mood disorder, Movement disorders, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Status marmoratus, Still diseaseView all (3 more) |
