Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8711 to 8720 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8711
NLR family pyrin domain containing 5
CLR19.8, MATER, NALP5, OZEMA19, PAN11, PYPAF8
Aplasia cutis congenita with epibulbar dermoids, Atrophic macular degeneration, Coronary artery disease, Dental caries, Oocyte maturation defect

8712
NLR family pyrin domain containing 6
AVR, CLR11.4, NALP6, NAVR, NAVR/AVR, PAN3, PYPAF5
Aortic stenosis, Cataract, Meningioma, Uterine fibroid

8713
NLR family pyrin domain containing 7
CLR19.4, HYDM, NALP7, NOD12, PAN7, PYPAF3
Alzheimer disease, Hydatidiform mole, Partial hydatidiform mole

8714
NLR family pyrin domain containing 8
CLR19.2, NALP8, NOD16, PAN4
Anorectal malformation, Obesity

8715
NLR family pyrin domain containing 9
CLR19.1, NALP9, NOD6, PAN12
Major depressive disorder, Night blindness, congenital stationary

8716
Neuromedin B
-
Dilated cardiomyopathy, Obesity, Pruritus, Schizophrenia

8717
Neuromedin B receptor
BB1, BB1R, BRS1, NMB-R
Bell's palsy, Breast neoplasms, Color vision deficiency, Lung cancer, Peptic ulcer disease

8718
NMD3 ribosome export adaptor
CGI-07
Schizophrenia

8719
NME/NM23 nucleoside diphosphate kinase 1
AWD, GAAD, NB, NBS, NDKA, NDPK-A, NDPKA, NM23, NM23-H1
Hepatocellular carcinoma, Cardiomyopathy, Colorectal neoplasms, Hypertrophic cardiomyopathy, Hypoxia, Myocardial infarction

8720
NME1-NME2 readthrough
NM23-LV, NMELV
Atrial fibrillation