|
481
|
|
|
Nuclear receptor coactivator 1 |
F-SRC-1, KAT13A, RIP160, SRC1, bHLHe42, bHLHe74 |
Atrial fibrillation, Breast cancer, Breast neoplasm, Diffuse large b-cell lymphoma, Endometriosis, Lung cancer, Nasal polyp, Oligodendroglioma, Prostatic neoplasm, Sjogren syndrome, Squamous cell carcinoma, Diabetes mellitus, type 1, Diabetes mellitus, type 2 |
|
482
|
|
|
NUMB endocytic adaptor protein |
C14orf41, S171, c14_5527 |
|
|
483
|
|
|
Nucleolar protein 4 |
CT125, HRIHFB2255, NOLP |
Asthma, Bipolar disorder, Insomnia, Major depressive disorder, Metabolic syndrome, Neurotic disorder, Obesity, Parkinson disease, Willis-ekbom disease, Schizophrenia, Diabetes mellitus, type 2 |
|
484
|
|
|
NSF attachment protein gamma |
GAMMASNAP |
|
|
485
|
|
|
Neuropilin 2 |
NP2, NPN2, PRO2714, VEGF165R2 |
Androgenetic alopecia, Autism, Obstructive pulmonary disease, Diabetic neuropathy, Meningitis, Ovarian cancer, Scoliosis, Seizures, Diabetes mellitus, type 2, Viral pneumonia |
|
486
|
|
|
Neuropilin 1 |
BDCA4, CD304, NP1, NRP, VEGF165R |
Alzheimer disease, Color vision deficiency, Congenital heart disease, Coronary artery disease, Crohn disease, Dementia, Digestive system disease, Endometriosis, Liver disease, Major depressive disorder, Metabolic syndrome, Migraine, Obstructive sleep apnea syndrome, Pancreatic neoplasm, Pelvic organ prolapse, Prostatic neoplasm, Schizophrenia, Small cell lung carcinoma, Diabetes mellitus, type 1, Diabetes mellitus, type 2View all (5 more) |
|
487
|
|
|
Nuclear receptor subfamily 1 group I member 2 |
BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR |
Barrett esophagus, Calcinosis, Diabetes mellitus, Esophageal neoplasm, Fatty liver, Fatty liver, alcoholic, Hepatomegaly, Female infertility, Metabolic syndrome, Obesity, Osteosarcoma, Scoliosis |
|
488
|
|
|
- |
- |
Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Dementia, Developmental delay, Epilepsy, Hearing impairment, Leber hereditary optic neuropathy, Macular degeneration, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy with hearing impairment, Optic atrophy, Optic neuritis, Optic neuropathy, Parkinson disease, Peripheral neuropathy, Retinitis pigmentosa, Schizophrenia, Postaxial polydactyly, Venous thromboembolismView all (7 more) |
|
489
|
|
|
- |
- |
Auditory neuropathy, Blindness, Dysarthria, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial disease, Optic atrophy, Paresthesia, Parkinson disease, Spinal muscular atrophy |
|
490
|
|
|
- |
- |
|
