|
51
|
|
|
Nucleus accumbens associated 1 |
BEND8, BTBD14B, BTBD30, NAC-1, NAC1, NECFM |
|
|
52
|
|
|
NLR family pyrin domain containing 3 |
AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1, DFNA34, FCAS, FCAS1, FCU, KEFH, MWS, NALP3, PYPAF1 |
Anaphylaxis, Cerebral arteriovenous malformations, Asbestosis, Ataxia, Autoinflammatory syndrome, Infantile neurological cutaneous and articular syndrome, Kidney disease, Coronary artery disease, Crohn disease, Autosomal dominant sensorineural deafness, Desbuquois syndrome, Cold autoinflammatory syndrome, Hearing loss, Diabetes mellitus, type 2, Keratitis, Kidney failure, Colorectal adenoma, Multiple sclerosis, Nonalcoholic fatty liver disease, Pericardial effusion, Pulmonary edema, Sepsis, Venous thromboembolismView all (8 more) |
|
53
|
|
|
NUS1 dehydrodolichyl diphosphate synthase subunit |
C6orf68, CDG1AA, MGC:7199, MRD55, NgBR, TANGO14 |
Bladder exstrophy, Congenital disorder of glycosylation, Coronary artery disease, Diabetes mellitus type 2, Fatty liver, Fatty liver, alcoholic, Hyperglycemia, Diabetes mellitus, type 2, Intellectual developmental disorder, Melanoma, Metabolic syndrome, Developmental and epileptic encephalopathy, Perisylvian syndrome, Progressive myoclonic epilepsy, Schizophrenia |
|
54
|
|
|
Niban apoptosis regulator 1 |
C1orf24, FAM129A, GIG39, NIBAN |
|
|
55
|
|
|
Neurexophilin and PC-esterase domain family member 1 |
FAM55A |
|
|
56
|
|
|
Non-coding RNA in the aldehyde dehydrogenase 1A pathway |
LINC00284, NCRNA00284 |
|
|
57
|
|
|
NIPA magnesium transporter 1 |
FSP3, SLC57A1, SPG6 |
|
|
58
|
|
|
N-terminal asparagine amidase |
PNAA, PNAD |
|
|
59
|
|
|
NLR family pyrin domain containing 8 |
CLR19.2, NALP8, NOD16, PAN4 |
|
|
60
|
|
|
NADH:ubiquinone oxidoreductase subunit A11 |
B14.7, CI-B14.7, MC1DN14 |
|
