JUP junction plakoglobin [ Homo sapiens (human) ]
Source: NCBI Gene (ID 3728)
Source: NCBI Gene (ID 3728)
Symbol: JUP
Full name: junction plakoglobin
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: CTNNG; DP3; DPIII; PDGB; PG; PKGB
Summary: This gene encodes a major cytoplasmic protein which is the only known constituent common to submembranous plaques of both desmosomes and intermediate junctions. This protein forms distinct complexes with cadherins and desmosomal cadherins and is a member of the catenin family since it contains a distinct repeating amino acid motif called the armadillo repeat. Mutation in this gene has been associated with Naxos disease. Alternative splicing occurs in this gene; however, not all transcripts have been fully described. [provided by RefSeq, Jul 2008]
Expression: Broad expression in skin (RPKM 236.9), esophagus (RPKM 189.1) and 16 other tissues
Orthologs: mouse
Gene size: 32103bp
Exon count: 19