Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8541 to 8550 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8541
NADH:ubiquinone oxidoreductase subunit V3
CI-10k, CI-9KD
Bipolar disorder, Major depressive disorder, Psychotic disorders

8542
Nebulin
AMC6, NEB177D, NEM2
Arthrogryposis multiplex congenita, Nebulin-related myopathy, Nemaline myopathy, Congenital neck anomaly, Congenital muscular dystrophy, Congenital structural myopathy, Deglutition disorder, Distal nebulin myopathy, Non-immune hydrops fetalis, Major depressive disorder, Muscular dystrophy, Peripheral neuropathy, Congenital nemaline myopathy, Squamous cell carcinoma, Diabetes mellitus type 2

8543
Nebulette
C10orf113, LASP2, LNEBL, bA165O3.1
Atrial fibrillation, Breast cancer, Cardiac arrest, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Obstructive pulmonary disease, Color vision deficiency, Conotruncal cardiac defect, Coronary aneurysm, Digeorge syndrome, Eosinophilia, Heart failure, Hypertrophic cardiomyopathy, Metabolic syndrome
View all (8 more)

8544
N-terminal EF-hand calcium binding protein 1
EFCBP1, STIP-1
Alzheimer disease, Dementia

8545
N-terminal EF-hand calcium binding protein 2
EFCBP2, stip-2
Color vision deficiency, Corneal astigmatism, Rheumatoid arthritis

8546
NECAP endocytosis associated 1
DEE21, EIEE21
Developmental and epileptic encephalopathy

8547
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

8548
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
View all (17 more)

8549
Nectin cell adhesion molecule 3
CD113, CDW113, NECTIN-3, PPR3, PRR3, PVRL3, PVRR3
Congenital cataract, Stroke, Teratozoospermia

8550
Nectin cell adhesion molecule 4
EDSS1, LNIR, PRR4, PVRL4, nectin-4
Color vision deficiency, Ectodermal dysplasia