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TGM5

Official Full Name
transglutaminase 5
Organism
Homo sapiens
GeneID
9333
Background
This gene encodes a member of the transglutaminase family. The encoded protein catalyzes formation of protein cross-links between glutamine and lysine residues, often resulting in stabilization of protein assemblies. This reaction is calcium dependent. Mutations in this gene have been associated with acral peeling skin syndrome. [provided by RefSeq, Oct 2009]
Synonyms
TGX; PSS2; TGM6; TGMX; TG(X); TGASE5; TGASEX;

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