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Search Thermo Fisher Scientific
Sequence of this protein is as follows: MAQEEGGSLP EVRARVRAAH GIPDLAQKLH FYDRWAPDYD QDVATLLYRA PRLAVDCLTQ ALPGPPHSAL ILDVACGTGL VAAELRAPGF LQLHGVDGSP GMLEQARAPG LYQRLSLCTL GQEPLPSPEG TFDAVLIVGA LSDGQVPCNA IPELHVTKPG GLVCLTTRTN WSNLQYKEAL EATLDRLEQA GMWEGLVAWP VDRLWTAGSW LPPSWWWYPA SLPRMASSPA LSTCTESGRR PRLRK
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]
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Protein Aliases: Methyltransferase-like protein 27; Williams-Beuren syndrome chromosomal region 27 protein
Gene Aliases: METTL27; WBSCR27
UniProt ID: (Human) Q8N6F8
Entrez Gene ID: (Human) 155368
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