111
|
|
|
Nuclear receptor coactivator 7 |
ERAP140, ESNA1, NCOA7-AS, Nbla00052, Nbla10993, TLDC4, dJ187J11.3 |
|
112
|
|
|
Nuclear receptor corepressor 1 |
N-CoR, N-CoR1, PPP1R109, TRAC1, hN-CoR |
Autism, Breast neoplasms, Transitional cell carcinoma, Neurodevelopmental disorder, Developmental delay, Endometriosis, Glioblastoma, Hyperbilirubinemia, Lewy body disease, Liver neoplasms, Mitochondrial complex deficiency, Non-specific syndromic intellectual disability, Prostatic neoplasms, Rhabdomyolysis, Urinary bladder neoplasms |
113
|
|
|
Nuclear receptor corepressor 2 |
CTG26, N-CoR2, SMAP270, SMRT, SMRTE, SMRTE-tau, TNRC14, TRAC, TRAC-1, TRAC1 |
Alzheimer disease, Androgenetic alopecia, Atrial fibrillation, Cardioembolic stroke, Crohn disease, Hypertension, Malunion fracture, Metabolic syndrome, Migraine, Multiple sclerosis, Myocardial infarction, Neurotic disorder, Osteoarthritis, Schizophrenia, Diabetes mellitus type 2, Ulcerative colitis, Uterine fibroidView all (2 more) |
114
|
|
|
Natural cytotoxicity triggering receptor 1 |
CD335, LY94, NK-p46, NKP46 |
|
115
|
|
|
Natural cytotoxicity triggering receptor 2 |
CD336, LY95, NK-p44, NKP44, dJ149M18.1 |
|
116
|
|
|
Natural cytotoxicity triggering receptor 3 |
1C7, CD337, LY117, MALS, NKp30 |
Asthma, Atrial fibrillation, Autoimmune thyroid disease, Coronary artery disease, Crohn disease, Hyperlipidemia, Hypertension, Hypothyroidism, Inflammatory bowel disease, Insomnia, Laryngeal carcinoma, Non-melanoma skin carcinoma, Psoriasis, Rheumatoid arthritis, Sarcoidosis, Systemic mastocytosis, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitisView all (4 more) |
117
|
|
|
Natural killer cell cytotoxicity receptor 3 ligand 1 |
B7-H6, B7H6, DKFZp686O24166 |
|
118
|
|
|
Neuronal calcium sensor 1 |
FLUP, FREQ |
|
119
|
|
|
Nicastrin |
ATAG1874 |
|
120
|
|
|
Mitochondrially encoded NADH dehydrogenase 1 |
MTND1 |
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Blepharoptosis, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Bipolar depression, Developmental regression, Diabetes mellitus type 2, Dysarthria, Dystonia, Global developmental delay, Leber hereditary optic neuropathy, Melas syndrome, Migraine, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Non-neoplastic peripheral nervous system disease, Obesity, Optic atrophy, Optic neuropathy, Parkinson disease, Hereditary parkinson disease, Peripheral neuropathy, Renal hypertension, Restrictive cardiomyopathy, Rheumatoid arthritis, Rod-cone dystrophy, Postaxial polydactyly, Wolfram syndromeView all (19 more) |
