|
181
|
|
|
NHL repeat containing 2 |
FINCA |
|
|
182
|
|
|
Negative regulator of reactive oxygen species |
ELLP3030, GARPL1, LRRC33, SENEBAC, UNQ3030 |
|
|
183
|
|
|
NHL repeat containing E3 ubiquitin protein ligase 1 |
EPM2A, EPM2B, MALIN, MELF2, bA204B7.2 |
Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Progressive myoclonic epilepsy, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Lafora disease, Non-hodgkins lymphoma, Ovarian cancer, Ovarian serous carcinoma, Pancreatic cancer, Prostate cancer, Psoriasis, Squamous cell carcinomaView all (5 more) |
|
184
|
|
|
Neuropeptide S receptor 1 |
ASRT2, GPR154, GPRA, NPSR, PGR14, VRR1 |
|
|
185
|
|
|
Nuclear GTPase, germinal center associated |
C8orf80, HMFN0672, SLIP-GC, SLIPGC |
|
|
186
|
|
|
Nuclear receptor subfamily 3 group C member 2 |
MCR, MLR, MR, NR3C2VIT |
Alzheimer disease, Atrial fibrillation, Autism, Pseudohypoaldosteronism, Cardiomyopathy, Cervical cancer, Major depressive disorder, Endometriosis, Heart failure, Hypertension, Insomnia, Keratoconus, Depression, Myocardial infarction, Pseudohypoparathyroidism, Rolandic epilepsy, Schizophrenia, Ventricular dysfunctionView all (3 more) |
|
187
|
|
|
NR2F1 regulatory antisense RNA 1 |
NAS1 |
|
|
188
|
|
|
NOTCH regulated ankyrin repeat protein |
- |
|
|
189
|
|
|
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, Experimental diabetes, Diabetes mellitus type 2, Dysarthria, 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, Retinitis pigmentosa, Toxic shock syndrome, Postaxial polydactyly, Wolfram syndromeView all (20 more) |
|
190
|
|
|
Mitochondrially encoded NADH dehydrogenase 2 |
MTND2 |
Alzheimer disease, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Myocardial infarction, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Parkinson disease, Retinitis pigmentosa, Postaxial polydactylyView all (1 more) |
