Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8701 to 8710 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8701
NLR family CARD domain containing 3
CLR16.2, NOD3
Hepatocellular carcinoma, Diabetes mellitus type 2

8702
NLR family CARD domain containing 4
AIFEC, CARD12, CLAN, CLAN1, CLANA, CLANB, CLANC, CLAND, CLR2.1, FCAS4, IPAF
Autoinflammation with infantile enterocolitis, Autoinflammatory syndrome, Cryopyrin-associated periodic syndrome, Cold autoinflammatory syndrome

8703
NLR family CARD domain containing 5
CLR16.1, NOD27, NOD4
Bipolar disorder, Fatty liver, alcoholic, Major depressive disorder, Metabolic syndrome, Multiple sclerosis, Neutropenia, Schizophrenia, Diabetes mellitus type 2

8704
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

8705
NLR family pyrin domain containing 10
CLR11.1, NALP10, NOD8, PAN5, PYNOD
Eczema

8706
NLR family pyrin domain containing 11
CLR19.6, NALP11, NOD17, PAN10, PYPAF6, PYPAF7
Tourette syndrome, Multiple sclerosis

8707
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

8708
NLR family pyrin domain containing 2
CLR19.9, NALP2, NBS1, OZEMA18, PAN1, PYPAF2
Alzheimer disease, Oocyte maturation defect, Venous thromboembolism

8709
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)

8710
NLR family pyrin domain containing 4
CLR19.5, CT58, NALP4, PAN2, PYPAF4, RNH2
Autism, Insomnia, Macular degeneration