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This protein encoded by this gene belongs to the apyrase family. It functions as a calcium-dependent nucleotidase with a preference for UDP. Mutations in this gene are associated with Desbuquois dysplasia with hand anomalies.
5830420C20Rik; Apy1h; apyrase 1, homolog (C. lectularius); apyrase homolog; Ca2+-dependent endoplasmic reticulum nucleoside diphosphatase; calcium activated nucleotidase 1; Cant1; D11Bwg0554e; DBQD; DBQD1; EC 3.6.1.6; ectonucleoside triphosphate diphosphohydrolase 8; Entpd8; galectin-3-binding protein; soluble calcium-activated nucleotidase 1; lectin, galactoside-binding, soluble, 3 binding protein; LGALS3BP; micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification; putative MAPK-activating protein PM09; Putative NF-kappa-B-activating protein 107; SCAN1; SCAN-1; SHAPY; soluble Ca-activated nucleotidase, isozyme 1; soluble calcium-activated nucleotidase 1; soluble calcium-activated nucleotidase SCAN-1; srapy
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