Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "N"
501 to 510 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

501
NFS1 cysteine desulfurase
COXPD52, HUSSY-08, IscS, NIFS
Basal cell carcinoma, Combined oxidative phosphorylation deficiency, Coronary artery disease, Non-melanoma skin carcinoma

502
Nuclear export mediator factor
IDDSAPN, NY-CO-1, RQC2, SDCCAG1
Autism, Osteopetrosis, Gestational diabetes, Intellectual developmental disorder speech peripheral neuropathy, Diabetes mellitus, type 1, Diabetes mellitus, type 2

503
Neuralized E3 ubiquitin protein ligase 1
NEUR1, NEURL, RNF67, bA416N2.1, neu, neu-1
Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Colorectal neoplasm, Major depressive disorder, Schizophrenia, Uterine fibroid

504
Nexilin F-actin binding protein
CDM2M, CMH20, NELIN
Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Heart failure, Hypertrophic cardiomyopathy, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome

505
NLR family pyrin domain containing 12
CLR19.3, FCAS2, NALP12, PAN6, PYPAF7, RNO, RNO2
Autoimmune interstitial lung disease-arthritis syndrome, Autoinflammatory syndrome, Bell's palsy, Renal cell carcinoma, Cold autoinflammatory syndrome, Schizophrenia

506
NIMA related kinase 9
APUG, LCCS10, NC, NERCC, NERCC1
Arthrogryposis with perthes disease and gaze palsy, Congenital omphalocele, Coronary artery disease, Desbuquois syndrome, Lethal congenital contracture syndrome

507
NADH:ubiquinone oxidoreductase complex assembly factor 2
B17.2L, MC1DN10, MMTN, NDUFA12L, mimitin
Alzheimer disease, Attention deficit hyperactivity disorder, Brain dopamine-serotonin vesicular transport disease, Cannabis abuse, Cockayne syndrome, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Parkinson disease, Schizophrenia, Scoliosis, Substance abuse, Vacterl association

508
Nuclear assembly factor 1 ribonucleoprotein
PFBMFT7
Glioma, Lung cancer, Myeloproliferative disorder, Pulmonary fibrosis, Telomere-related pulmonary fibrosis and/or bone marrow failure, Schizophrenia, Squamous cell carcinoma

509
Noggin
SYM1, SYNS1, SYNS1A
Androgenetic alopecia, Brachydactyly, Common wart, Craniosynostosis, Proximal symphalangism, Desbuquois syndrome, Hemimelia of limb, Huntington disease, Hyperopia, Multiple synostoses syndrome, Orofacial cleft, Osteoarthritis, Retinal detachment, Sleep apnea, Amyotrophic lateral sclerosis

510
NUMB like endocytic adaptor protein
CAG3A, CTG3a, NBL, NUMB-R, NUMBLIKE, NUMBR, TNRC23
Angioedema, Gestational diabetes, Lung cancer, Schizophrenia, Squamous cell carcinoma