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"
201 to 210 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
N-terminal EF-hand calcium binding protein 1
EFCBP1, STIP-1
Alzheimer disease, Dementia

202
N-terminal EF-hand calcium binding protein 2
EFCBP2, stip-2
Color vision deficiency, Corneal astigmatism, Rheumatoid arthritis

203
NECAP endocytosis associated 1
DEE21, EIEE21
Developmental and epileptic encephalopathy

204
Nectin cell adhesion molecule 1
CD111, CLPED1, ED4, HIgR, HV1S, HVEC, OFC7, PRR, PRR1, PVRL1, PVRR, PVRR1, SK-12, nectin-1
Cleft lip and cleft of alveolar process of maxilla, Cleft lip/palate-ectodermal dysplasia syndrome, Cleft palate, Cleft lip and palate, Cleft lip, Complete unilateral cleft lip, Ectodermal dysplasia, Obsessive-compulsive disorder, Orofacial cleft, Tourette syndrome

205
Nectin cell adhesion molecule 2
CD112, HVEB, PRR2, PVRL2, PVRR2
Alzheimer disease, Aortic aneurysm, Atherosclerosis, Atrial fibrillation, Breast neoplasms, Cardiovascular disease, Cerebral amyloid angiopathy, Cerebral palsy, Cognition disorder, Coronary artery disease, Dementia, Diabetic neuropathy, Dyslipidemias, Frontotemporal dementia, Gastroesophageal reflux disease
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206
Nectin cell adhesion molecule 3
CD113, CDW113, NECTIN-3, PPR3, PRR3, PVRL3, PVRR3
Congenital cataract, Stroke, Teratozoospermia

207
Nectin cell adhesion molecule 4
EDSS1, LNIR, PRR4, PVRL4, nectin-4
Color vision deficiency, Ectodermal dysplasia

208
NEDD1 gamma-tubulin ring complex targeting factor
GCP-WD, TUBGCP7
Cerebral amyloid angiopathy, Internet addiction disorder

209
NEDD4 E3 ubiquitin protein ligase
NEDD4-1, RPF1
Autism, Bipolar disorder, Cataract, Coronary artery disease, Dupuytren contracture, Myocardial ischemia, Open angle glaucoma, Rheumatoid arthritis, Stevens-johnson syndrome, Testicular carcinoma, Testicular germ cell tumor

210
NEDD4 like E3 ubiquitin protein ligase
NEDD4-2, NEDD4.2, PVNH7, RSP5, hNEDD4-2
Appendicitis, Asthma, Atrial fibrillation, Autism, Dilated cardiomyopathy, Cleft palate, Endometriosis, Heart failure, Periventricular nodular heterotopia, Hypertension, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Major depressive disorder, Migraine, Nonalcoholic fatty liver disease
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