Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "N"

201 to 210 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
201	4671	NAIP	NLR family apoptosis inhibitory protein	BIRC1, NLRB1, psiNAIP	Proximal spinal muscular atrophy, Spinal muscular atrophy
202	4681	NBL1	NBL1, DAN family BMP antagonist	D1S1733E, DAN, DAND1, NB, NO3	Bronchopulmonary dysplasia
203	4683	NBN	Nibrin	AT-V1, AT-V2, ATV, NBS, NBS1, P95, hNbs1	Aplastic anemia, Prostate cancer, Hereditary breast and ovarian cancer syndrome, Hereditary breast cancer, Hypertension, Acute lymphoblastic leukemia, Lissencephaly, Metabolic syndrome, Microcephaly, Prostatic neoplasm, Rhabdomyosarcoma, Stomatitis
204	4684	NCAM1	Neural cell adhesion molecule 1	CD56, MSK39, NCAM	Anorexia nervosa, Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cannabis abuse, Central nervous system cancer, Bipolar depression, Major depressive disorder, Gastroesophageal reflux disease, Glioblastoma, Glioma, Insomnia, Irritable bowel syndrome, Depression View all (9 more)
205	4685	NCAM2	Neural cell adhesion molecule 2	NCAM21	Attention deficit hyperactivity disorder, Coronary artery disease, Endometrial cancer, Ovarian epithelial cancer, Obesity, Osteoarthritis, Ovarian cancer, Severe acute respiratory syndrome, Substance abuse, Ventricular septal defect
206	4688	NCF2	Neutrophil cytosolic factor 2	NCF-2, NOXA2, P67-PHOX, P67PHOX	Alzheimer disease, Rheumatoid arthritis, Autoimmune musculoskeletal system disorder, Celiac disease, Granulomatous disease, Myositis, Systemic lupus erythematosus, Systemic sclerosis
207	4689	NCF4	Neutrophil cytosolic factor 4	CGD3, NCF, P40PHOX, SH3PXD4	Asthma, Eczema, Granulomatous disease, Crohn disease, Heart disease, Inflammatory bowel disease, Multiple sclerosis, Respiratory system disease, Rheumatoid arthritis, Ulcerative colitis
208	4690	NCK1	NCK adaptor protein 1	NCK, NCKalpha, nck-1	Lymphocytic leukemia, Hodgkin lymphoma, Multiple myeloma, Myocardial infarction, Nephrotic syndrome, Neurotic disorder, Proteinuria
209	4691	NCL	Nucleolin	C23, Nsr1	Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Myocardial ischemia
210	4692	NDN	Necdin, MAGE family member	HsT16328, PWCR	Carcinoma, Oligodendroglioma, Prader-willi syndrome, Psychiatric disorders

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