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Antibody detects endogenous levels of total CANT1.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: apyrase 1, homolog (C. lectularius); Apyrase homolog; Ca2+-dependent endoplasmic reticulum nucleoside diphosphatase; EC 3.6.1.6; ectonucleoside triphosphate diphosphohydrolase 8; micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification; Putative MAPK-activating protein PM09; Putative NF-kappa-B-activating protein 107; SCAN-1; soluble Ca-activated nucleotidase, isozyme 1; Soluble calcium-activated nucleotidase 1; soluble calcium-activated nucleotidase SCAN-1
Gene Aliases: 5830420C20Rik; Apy1h; CANT1; D11Bwg0554e; DBQD; DBQD1; Entpd8; SCAN-1; SCAN1; SHAPY; Srapy
UniProt ID: (Human) Q8WVQ1, (Mouse) Q8VCF1, (Rat) Q8K4Y7
Entrez Gene ID: (Human) 124583, (Mouse) 76025, (Rat) 246272
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