Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "N"

391 to 400 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
391	58157	NGB	Neuroglobin	-	Conotruncal cardiac defect
392	5818	NECTIN1	Nectin cell adhesion molecule 1	CD111, CLPED1, ED4, HIgR, HV1S, HVEC, OFC7, PRR, PRR1, PVRL1, PVRR, PVRR1, SK-12, nectin-1	Ectodermal dysplasia, Obsessive-compulsive disorder, Orofacial cleft, Tourette syndrome
393	5819	NECTIN2	Nectin cell adhesion molecule 2	CD112, HVEB, PRR2, PVRL2, PVRR2	Alzheimer disease, Aortic aneurysm, Atherosclerosis, Atrial fibrillation, Breast neoplasm, Cardiovascular disease, Cerebral amyloid angiopathy, Cerebral palsy, Cognition disorder, Coronary artery disease, Dementia, Diabetic neuropathy, Dyslipidemias, Frontotemporal dementia, Gastroesophageal reflux disease View all (17 more)
394	58484	NLRC4	NLR family CARD domain containing 4	AIFEC, CARD12, CLAN, CLAN1, CLANA, CLANB, CLANC, CLAND, CLR2.1, FCAS4, IPAF	Autoinflammation with infantile enterocolitis, Autoinflammatory syndrome, Enterocolitis, Cold autoinflammatory syndrome
395	59277	NTN4	Netrin 4	PRO3091	Contact dermatitis, Gastroesophageal reflux disease, Gout, Kidney cancer, Pelvic organ prolapse, Psychiatric disorders, Severe acute respiratory syndrome
396	594857	NPS	Neuropeptide S	-	Amyotrophic lateral sclerosis, Anxiety disorder, Carotid artery disease, Central nervous system cancer, Major depressive disorder, Glioma, Hyperkinesia, Insomnia, Depression, Obstructive sleep apnea syndrome, Ocular hypotension, Schizophrenia
397	60506	NYX	Nyctalopin	CLRP, CSNB1, CSNB1A, CSNB4, NBM1	Night blindness, congenital stationary, Oguchi disease, Retinitis pigmentosa
398	63974	NEUROD6	Neuronal differentiation 6	Atoh2, MATH2, Math-2, NEX1M, Nex1, bHLHa2	Alzheimer disease, Attention deficit hyperactivity disorder, Dementia, Major depressive disorder, Substance abuse
399	64067	NPAS3	Neuronal PAS domain protein 3	MOP6, PASD6, bHLHe12	Alzheimer disease, Ankylosing spondylitis, Anorexia nervosa, Asthma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bronchial disease, Obstructive pulmonary disease, Colorectal cancer, Dementia, Endometrial neoplasm, Heart failure, Insomnia, Major depressive disorder View all (16 more)
400	64127	NOD2	Nucleotide binding oligomerization domain containing 2	ACUG, BLAU, BLAUS, CARD15, CD, CLR16.3, IBD1, NLRC2, NOD2B, PSORAS1, YAOS	Ankylosing spondylitis, Asthma, Autoinflammatory syndrome, Behcet disease, Bipolar disorder, Bronchiolitis obliterans, Cardiomyopathy, Ischemic heart disease, Obstructive airway disease, Ulcerative colitis, Colorectal adenoma, Coronary artery disease, Crohn disease, Dermatitis, Gastritis View all (19 more)

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