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GLDN

Official Full Name
gliomedin
Organism
Homo sapiens
GeneID
342035
Background
This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017]
Synonyms
CLOM; COLM; CRGL2; CRG-L2; LCCS11; UNC-112; UNC-122;

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