|
481
|
|
|
Nuclear receptor coactivator 1 |
F-SRC-1, KAT13A, RIP160, SRC1, bHLHe42, bHLHe74 |
|
|
482
|
|
|
NUMB endocytic adaptor protein |
C14orf41, S171, c14_5527 |
|
|
483
|
|
|
Nucleolar protein 4 |
CT125, HRIHFB2255, NOLP |
|
|
484
|
|
|
NSF attachment protein gamma |
GAMMASNAP |
|
|
485
|
|
|
Neuropilin 2 |
NP2, NPN2, PRO2714, VEGF165R2 |
|
|
486
|
|
|
Neuropilin 1 |
BDCA4, CD304, NP1, NRP, VEGF165R |
|
|
487
|
|
|
Nuclear receptor subfamily 1 group I member 2 |
BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR |
Adenocarcinoma, Barrett epithelium, Barrett esophagus, Carcinoma, Diabetes mellitus, Esophagus neoplasm, Fatty liver, Fibroatheroma, Metabolic syndrome, Obesity, Osteosarcoma, Subfertility |
|
488
|
|
|
- |
- |
Addison`s disease, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cardiomyopathy, Cataract, Cerebral cortical atrophy, Congestive heart failure, Demyelinating neuropathy, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hereditary optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Leber plus disease, Leigh syndrome, Liver failure, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial complex deficiency, Mitochondrial diseases, Mitochondrial myopathy, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Nystagmus, Optic atrophy, Pancreatitis, Polyneuropathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Retinitis pigmentosa, Rod-cone dystrophy, Schizophrenia, Seizure, Sensorimotor neuropathy, Thyroiditis, Ventricular preexcitation, West syndromeView all (59 more) |
|
489
|
|
|
- |
- |
Addison`s disease, Wolff-parkinson-white syndrome, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cardiomyopathy, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hereditary leber optic atrophy, Hereditary optic atrophy, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Leber plus disease, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial myopathy, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nervous system diseases, Nyctalopia, Nystagmus, Optic atrophy, Oxyphilic adenoma, Pancreatitis, Parkinson disease, Polyneuropathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal telangiectasia, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Thyroiditis, Ventricular preexcitation, West syndromeView all (63 more) |
|
490
|
|
|
- |
- |
|
