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TM2D1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | TM2D1, BBP, TM2 domain containing 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 610080; MGI: 2137022; HomoloGene: 12928; GeneCards: TM2D1; OMA:TM2D1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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TM2 domain containing 1 is a protein that in humans is encoded by the TM2D1 gene. [5]
The protein encoded by this gene is a beta-amyloid peptide-binding protein. It contains a structural module related to that of the seven transmembrane domain G protein-coupled receptor superfamily and known to be important in heterotrimeric G protein activation. Beta-amyloid peptide has been established to be a causative factor in neuron death and the consequent diminution of cognitive abilities observed in Alzheimer's disease. This protein may be a target of neurotoxic beta-amyloid peptide, and may mediate cellular vulnerability to beta-amyloid peptide toxicity through a G protein-regulated program of cell death. Several transcript variants have been found for this gene.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.