Your search for "megf8" returned 291 TaqMan® SNP Genotyping Assays
multiple EGF like domains 8
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]
AW049492, B2B1702CLO, B2B288CLO, C19ORF49, CRPT2, EGFL4, M687DDG, MEGF8, MKIAA0817, SBP1
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