61
|
|
|
Neuron navigator 1 |
POMFIL3, STEERIN1, UNC53H1 |
Aortic stenosis, Aortic valve disease, Attention deficit hyperactivity disorder, Autism, Cardiovascular disease, Celiac disease, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Gout, Insomnia, Interstitial lung disease, Lung cancer, Metabolic syndrome, Mouth disease, Obesity, Prostate cancer, Schizophrenia, Diabetes mellitus type 2View all (4 more) |
62
|
|
|
Neuron navigator 2 |
HELAD1, POMFIL2, RAINB1, STEERIN2, UNC53H2 |
Alzheimer disease, Autoimmune neurological syndrome, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autoimmune thrombocytopenic purpura, Central nervous system cancer, Color vision deficiency, Coronary aneurysm, Dementia, Dry eye syndrome, Glioblastoma, Glioma, Obesity, Paralytic strabismus, Peripheral arterial disease, Scoliosis, Sjogren syndrome, Vascular dementia, Venous thromboembolismView all (5 more) |
63
|
|
|
Neuron navigator 3 |
NEDSFB, POMFIL1, STEERIN3, unc53H3 |
Appendicitis, Autism, Renal cell carcinoma, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Colorectal cancer, Neurodevelopmental disorder, Diabetic neuropathy, Endometrial cancer, Endometrial neoplasms, Eye disease, Gastroesophageal reflux disease, Hearing impairment, Major depressive disorder, Mood disorder, Non-specific syndromic intellectual disability, Obesity, Schizophrenia, Sleep apnea, Systemic mastocytosis, TrigonocephalyView all (7 more) |
64
|
|
|
NAD(P)HX dehydratase |
CARKD, LP3298, PEBEL2 |
|
65
|
|
|
NAD(P)HX epimerase |
AIBP, APOA1BP, PEBEL, YJEFN1 |
|
66
|
|
|
NBAS subunit of NRZ tethering complex |
ILFS2, NAG, SOPH |
Alzheimer disease, Bipolar disorder, Bone fragility with contractures, arterial rupture, and deafness, Central nervous system cancer, Conduct disorder, Desbuquois syndrome, Glioma, Leber congenital amaurosis, Liver failure, Major depressive disorder, Male reproductive organ cancer, Metabolic syndrome, Multiple sclerosis, Neurodevelopmental disorder, Obstructive sleep apnea syndrome, Optic atrophy, Osteoporosis-pseudoglioma syndrome, Ovarian cancer, Pituitary stalk interruption syndrome, Psychiatric disorders, Willis-ekbom disease, Retinitis pigmentosa, Schizophrenia, Scoliosis, Squamous cell carcinoma, Stomach neoplasms, Diabetes mellitus type 2View all (12 more) |
67
|
|
|
Negative regulator of P-body association |
LINC01420, NoBody |
|
68
|
|
|
Neurobeachin |
BCL8B, LYST2, NEDEGE |
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Nonsyndromic intellectual disability, Cerebellar, ocular, craniofacial, and genital syndrome, Color vision deficiency, Neurodevelopmental disorder, Developmental disability, Diverticulitis, Epilepsy, Intellectual developmental disorder, Interstitial lung disease, Liver cirrhosis, Migraine, Non-specific syndromic intellectual disability, Obstructive sleep apnea syndrome, Peripheral arterial disease, Substance abuse, Systemic sclerosis, Thrombocytopenia, Urinary bladder cancerView all (6 more) |
69
|
|
|
Neurobeachin like 1 |
A530083I02Rik, ALS2CR16, ALS2CR17 |
Alzheimer disease, Ischemic heart disease, Coronary artery disease, Hypertension, Myocardial infarction, Myocardial ischemia, Neurotic disorder, Obesity, Respiratory system disease, Scoliosis, Small vessel stroke, Stroke |
70
|
|
|
Neurobeachin like 2 |
BDPLT4, GPS |
|
