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The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012],similarity:Contains 12 Kelch repeats.,similarity:Contains 2 CUB domains.,similarity:Contains 4 laminin EGF-like domains.,similarity:Contains 5 EGF-like domains.,similarity:Contains 7 PSI domains.,
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