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"
361 to 370 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
NLR family pyrin domain containing 1
AIADK, CARD7, CIDED, CLR17.1, DEFCAP, DEFCAP-L/S, JRRP, MSPC, NAC, NALP1, PP1044, SLEV1, VAMAS1
Autoinflammation with arthritis and dyskeratosis, Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome, Corneal neovascularization, Crohn disease, Essential tremor, Hypotension, Irritable bowel syndrome, Keratitis, Lung cancer, Migraine, Non-small cell lung carcinoma, Ovarian cancer, Hypertension, Vitiligo

362
NLR family pyrin domain containing 10
CLR11.1, NALP10, NOD8, PAN5, PYNOD
Eczema

363
NLR family pyrin domain containing 11
CLR19.6, NALP11, NOD17, PAN10, PYPAF6, PYPAF7
Tourette syndrome, Multiple sclerosis

364
NLR family pyrin domain containing 12
CLR19.3, FCAS2, NALP12, PAN6, PYPAF7, RNO, RNO2
Autoimmune interstitial lung disease-arthritis syndrome, Autoinflammatory syndrome, Bell's palsy, Renal cell carcinoma, Cold autoinflammatory syndrome, Schizophrenia

365
NLR family pyrin domain containing 2
CLR19.9, NALP2, NBS1, OZEMA18, PAN1, PYPAF2
Alzheimer disease, Oocyte maturation defect, Venous thromboembolism

366
NLR family pyrin domain containing 3
AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1, DFNA34, FCAS, FCAS1, FCU, KEFH, MWS, NALP3, PYPAF1
Anaphylaxis, Cerebral arteriovenous malformations, Asbestosis, Ataxia, Autoinflammatory syndrome, Infantile neurological cutaneous and articular syndrome, Kidney disease, Cinca syndrome, Coronary artery disease, Crohn disease, Cryopyrin-associated periodic syndrome, Autosomal dominant sensorineural deafness, Desbuquois syndrome, Cold autoinflammatory syndrome, Hearing loss
View all (10 more)

367
NLR family pyrin domain containing 4
CLR19.5, CT58, NALP4, PAN2, PYPAF4, RNH2
Autism, Insomnia, Macular degeneration

368
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

369
NLR family pyrin domain containing 6
AVR, CLR11.4, NALP6, NAVR, NAVR/AVR, PAN3, PYPAF5
Aortic stenosis, Cataract, Meningioma, Uterine fibroid

370
NLR family pyrin domain containing 7
CLR19.4, HYDM, NALP7, NOD12, PAN7, PYPAF3
Alzheimer disease, Hydatidiform mole, Partial hydatidiform mole