Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "N"

291 to 300 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
291	4853	NOTCH2	Notch receptor 2	AGS2, HJCYS, hN2	Acroosteolysis, Alagille syndrome, Astrocytoma, Autism, Breast cancer, Breast neoplasm, Congenital anomalies of the kidney and urinary tract, Squamous cell carcinoma, Crohn disease, Melanoma, Dermatophytosis, Desbuquois syndrome, Diabetes mellitus, Diabetes mellitus type 2, Diabetic neuropathy View all (19 more)
292	4854	NOTCH3	Notch receptor 3	CADASIL, CADASIL1, CASIL, IMF2, LMNS	Auditory neuropathy, Autism, Breast neoplasm, Cadasil, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Pancreatic carcinoma, Squamous cell carcinoma, Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, Cerebrovascular disorder, Common migraine, Vascular dementia, Major depressive disorder, Esophageal squamous cell carcinoma, Partial lipodystrophy View all (9 more)
293	4855	NOTCH4	Notch receptor 4	INT3	Cerebral arteriovenous malformations, Asthma, Autism, Bipolar disorder, Breast neoplasm, Bronchiectasis, Pancreatic carcinoma, Squamous cell carcinoma, Celiac disease, Central serous retinopathy, Cervical cancer, Hepatitis b virus infection, Interstitial cystitis, Colorectal cancer, Crohn disease View all (29 more)
294	4861	NPAS1	Neuronal PAS domain protein 1	MOP5, PASD5, bHLHe11	Attention deficit hyperactivity disorder, Autism, Non-organic psychosis, Psychotic disorders, Schizophrenia
295	4862	NPAS2	Neuronal PAS domain protein 2	MOP4, PASD4, bHLHe9	Alzheimer disease, Autism, Benign thyroid gland neoplasm, Bipolar disorder, Chronobiology disorder, Creutzfeldt-jakob disease, Major depressive disorder, Essential tremor, Liver cirrhosis, Depression, Open angle glaucoma, Schizoaffective disorder, Schizophrenia, Seasonal affective disorder, Testicular azoospermia
296	4864	NPC1	NPC intracellular cholesterol transporter 1	NPC, POGZ, SLC65A1	Alzheimer disease, Apraxia, Ataxia, Atherosclerosis, Atrial fibrillation, Brucellosis, Cardiovascular disease, Cataplexy, Cerebellar ataxia, Coronary artery disease, Diabetes mellitus, Digestive system disease, Dysarthria, Gastrointestinal stromal tumor, Heart failure View all (7 more)
297	4867	NPHP1	Nephrocystin 1	JBTS4, NPH1, SLSN1	Appendicitis, Bardet-biedl syndrome, Congenital anomalies of the kidney and urinary tract, Aplasia of the vermis, Joubert syndrome, Nephronophthisis, Kidney disease, Leber congenital amaurosis, Nephronophthisis, familial juvenile, Neurotic disorder, Retinitis pigmentosa, Senior-loken syndrome
298	4868	NPHS1	NPHS1 adhesion molecule, nephrin	CNF, NPHN, nephrin	Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glomerulonephritis, Steroid-resistant nephrotic syndrome, Hyperhomocysteinemia, Kidney disease, Nephrotic syndrome, Oligodendroglioma, Proteinuria
299	4869	NPM1	Nucleophosmin 1	B23, NPM	Bone marrow failure syndromes, Dyskeratosis congenita, Myeloid leukemia, Promyelocytic leukemia, Primary cutaneous anaplastic large cell lymphoma, Stomach neoplasms
300	4878	NPPA	Natriuretic peptide A	ANF, ANP, ATFB6, ATRST2, CDD, CDD-ANF, CDP, PND	Aortic valve disease, Atrial fibrillation, Atrial standstill, Small cell carcinoma, Cardiomegaly, Cardiomyopathy, Ischemic heart disease, Coronary artery disease, Coronary stenosis, Vascular dementia, Heart failure, Hereditary atrial fibrillation, Hypercapnia, Hypertension, Renal hypertension View all (16 more)

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