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Invitrogen
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Immunogen sequence: HRPAPGRPPT HNAHNWRLGQ APANWYNDTY PLSPPQRTPA GIRYRIAVIA DLDTESRAQE ENTWFSYLKK GYLTLSDSGD KVAVEWDKDH GVLESHLAEK GRGMELSDLI VFNGKLYSVD DRTGVVYQIE GSKAVPWVIL SDGDGTVEKG FKAEWLAVKD ERLYVGGLGK
Positive Samples: U-251MG; Cellular Location: Endoplasmic reticulum membrane, Golgi apparatus, Golgi stack membrane, Single-pass type II membrane protein
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Apyrase homolog; Ca2+-dependent endoplasmic reticulum nucleoside diphosphatase; EC 3.6.1.6; 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
基因别名: CANT1; DBQD; DBQD1; SCAN-1; SCAN1; SHAPY
UniProt ID: (Human) Q8WVQ1
Entrez Gene ID: (Human) 124583