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Immunogen sequence: LIFASDACK NVTLHVPSKL DAEKLVGRVN LKECFTAANL IHSSDPDFQI LEDGSVYTTN TILLSSEKRS FTILLSNTEN QEKKKIFVFL EHQTKVLKKR HTKEKVLRRA KRRWAPIPCS MLENSLGPFP LFLQQVQSDT AQNYTIYYSI RGPGVDQEPR NLFYVERDTG NLYCTRPVDR EQYESFEIIA FATTPDGYTP ELPLPLIIKI EDENDNYPIF TEETYTFTIF ENCRVGTTVG QVCATDKDEP DTMHTRLKYS IIGQVPPSPT LFSMHPTTGV ITTTSSQLDR ELIDKYQLKI KVQDMDGQYF GLQTTSTCII NIDDVNDHLP TFTR (25-357 aa encoded by BC063291)
This gene encodes a member of the desmocollin protein subfamily. Desmocollins, along with desmogleins, are cadherin-like transmembrane glycoproteins that are major components of the desmosome. Desmosomes are cell-cell junctions that help resist shearing forces and are found in high concentrations in cells subject to mechanical stress. This gene is found in a cluster with other desmocollin family members on chromosome 18. Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia-11, and reduced protein expression has been described in several types of cancer. Alternative splicing results in multiple transcript variants.
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Protein Aliases: ARVC10; ARVD10; Cadherin family member 2; CDHF5; CDHF6; CMD1BB; Desmocollin-2; Desmocollin-3; desmoglein-2; desmoglein-3; Desmosomal glycoprotein II; desmosomal glycoprotein II/III; Desmosomal glycoprotein III; Epithelial type 2 desmocollin
Gene Aliases: ARVD11; AW228162; CDHF2; DG2; DGII/III; DSC2; Dsc2a; Dsc2b; DSC3
UniProt ID: (Human) Q02487, (Mouse) P55292
Entrez Gene ID: (Human) 1824, (Mouse) 13506
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