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MEGF8


Official Full Name
multiple EGF like domains 8
Organism
Homo sapiens
Gene ID
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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LV18067L human MEGF8 (NM_001410) lentivirus particles Inquiry
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SHH340279 shRNA set against Human MEGF8 (NM_001410.2) Inquiry
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