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MEGF8

Official Full Name
multiple EGF like domains 8
Organism
Homo sapiens
GeneID
1954
Background
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]
Synonyms
SBP1; CRPT2; EGFL4; C19orf49;

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