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DSG1 (Desmoglein 1) is a Protein Coding gene. Diseases associated with DSG1 include Erythroderma, Congenital, With Palmoplantar Keratoderma, Hypotrichosis, And Hyper-Ige and Palmoplantar Keratoderma I, Striate, Focal, Or Diffuse. Among its related pathways are Keratinization and Apoptotic execution phase. Gene Ontology (GO) annotations related to this gene include calcium ion binding and toxic substance binding. An important paralog of this gene is DSG4. DSG2 (Desmoglein 2) is a Protein Coding gene. Diseases associated with DSG2 include Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 and Cardiomyopathy, Dilated, 1Bb. Among its related pathways are Keratinization and Apoptotic execution phase. Gene Ontology (GO) annotations related to this gene include calcium ion binding and cell adhesive protein binding involved in bundle of His cell-Purkinje myocyte communication. An important paralog of this gene is DSG4.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Cadherin family member 4; Cadherin family member 5; desmoglein 1; desmoglein 1 beta; desmoglein 1 gamma; desmoglein 2; Desmoglein-1; Desmoglein-2; Desmosomal glycoprotein 1; DG1; DGI; DSG1; DSG1/2; DSG2; HDGC; Pemphigus foliaceus antigen
基因别名: AA408168; CDHF4; CDHF5; D18Ertd293e; DG1; DSG; DSG1; Dsg1b; Dsg1c; DSG2; EPKHE; EPKHIA; HDGC; PPKS1; SPPK1
UniProt ID: (Human) Q02413, (Bovine) Q03763, (Human) Q14126, (Mouse) O55111
Entrez Gene ID: (Human) 1828, (Bovine) 281131, (Human) 1829, (Bovine) 508151, (Rat) 291755, (Mouse) 13511, (Rat) 307562