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WBSCR27

Official Full Name
methyltransferase like 27
Organism
Homo sapiens
GeneID
155368
Background
This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]
Synonyms
METTL27; WBSCR27;

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