Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "N"
411 to 420 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

411
Non-coding RNA activated by DNA damage
LINC00657

412
Nicotinamide nucleotide adenylyltransferase 1
LCA9, NMNAT, PNAT1, SHILCA
Leber congenital amaurosis , Brain injuries, Cone dystrophy, Cone-rod dystrophy, Desbuquois syndrome, Developmental regression, Global developmental delay, Leber congenital amaurosis, Macular degeneration, Nystagmus, Optic atrophy, Retinal degeneration, Retinitis pigmentosa, Spondyloepiphyseal dysplasia, Wallerian degeneration

413
Nucleic acid binding protein 1
NABP1-OT1, OBFC2A, SOSS-B2, SSB2
Colorectal cancer, Multiple sclerosis, Oligodendroglioma, Open angle glaucoma, Osteoarthritis, Pancreatic cancer, Parkinson disease, Scoliosis

414
5'-nucleotidase domain containing 2
-
Attention deficit hyperactivity disorder, Autism, Cataract, Osteoarthritis

415
NDRG family member 4
BDM1, SMAP-8, SMAP8
Achromatopsia, Autism, Schizophrenia

416
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

417
Neutrophil cytosolic factor 1
CGD1, NCF-1, NCF-47K, NCF1A, NOXO2, SH3PXD1A, p47-phox, p47phox
Aortic aneurysm, Rheumatoid arthritis, Granulomatous disease, Diabetes mellitus, Experimental diabetes, Hypertension, Hypertrophic cardiomyopathy, Hypercholesterolemia, Intracranial aneurysm, Kidney failure, Systemic lupus erythematosus, Sjogren syndrome, Williams syndrome

418
-
-
Auditory neuropathy, Blindness, Dysarthria, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial disease, Optic atrophy, Paresthesia, Parkinson disease, Spinal muscular atrophy

419
-
-
Hepatocellular carcinoma, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Congenital cardiomyopathy, Developmental delay, Hearing impairment, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Myoclonic epilepsy with ragged red fibers, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, congenital hypomyelinating, Parkinson disease, Retinitis pigmentosa
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420
-
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Cerebellar ataxia, Cleft palate and bilateral cleft lip, Diabetes mellitus, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, congenital hypomyelinating, Leber hereditary optic neuropathy, Retinitis pigmentosa, Postaxial polydactyly