Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "N"
381 to 390 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

381
NME/NM23 family member 7
CFAP67, MN23H7, NDK 7, NDK7, nm23-H7
Blood coagulation disorder, Cardiac arrhythmia, Coronary artery disease, Endometriosis, Gastrointestinal stromal tumor, Lipoma, Myocardial infarction, Situs inversus, Thrombophilia, Venous thromboembolism

382
NME/NM23 family member 8
CILD6, DNAI8, HEL-S-99, NM23-H8, SPTRX2, TXNDC3, sptrx-2
Alzheimer disease, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Dupuytren contracture

383
NME/NM23 family member 9
NM23-H9, NXL2, TXL-2, TXL2, TXNDC6
Alzheimer disease, Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Coronary artery disease, Dyslexia, Hypertension, Gout, Metabolic syndrome, Myocardial infarction, Diabetes mellitus type 2

384
N-myc and STAT interactor
-
Liver cirrhosis, Diabetes mellitus type 2

385
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, Macular degeneration, Nystagmus, Optic atrophy, Retinal degeneration, Retinitis pigmentosa, Spondyloepiphyseal dysplasia, Wallerian degeneration

386
Nicotinamide nucleotide adenylyltransferase 2
C1orf15, PNAT2
Color vision deficiency, Vascular dementia, Obesity, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2

387
Nicotinamide nucleotide adenylyltransferase 3
FKSG76, PNAT-3, PNAT3
Polycystic ovary syndrome

388
NmrA like redox sensor 1
HSCARG, SDR48A1
Astrocytoma, Migraine, Osteoarthritis

389
Nicotinamide riboside kinase 1
C9orf95, NRK1, bA235O14.2
Colorectal cancer, Tourette syndrome

390
Nicotinamide riboside kinase 2
ITGB1BP3, MIBP, NRK2
Atrial fibrillation, Glaucoma