MEGF8 - 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]
NCBI Orthologs
How was this calculated?genes for:
Protein alignment
Download data
Species | Gene | Architecture | aa |
---|