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Immunogen sequence: MAQEEGGSLP EVRARVRAAH GIPDLAQKLH FYDRWAPDYD QDVATLLYRA PRLAVDCLTQ ALPGPPHSAL ILDVACGTGL VAAELRAPGF LQLHGVDGSP GMLEQAQAPG LYQRLSLCTL GQEPLPSPEG TFDAVLIVGA LSDGQVPCNA IPELHVTKPG GLVCLTTRTN SSNLQYKEAL EATLDRLEQA GMWEGLVAWP VDRLWTAGSW LPPSWRWYPA SLPRMASSPA LSTCTESGRR PRLRK; Positive Samples: HT-29, MCF7, Mouse lung
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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For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Methyltransferase-like protein 27; Williams-Beuren syndrome chromosomal region 27 protein; Williams-Beuren syndrome chromosome region 27 homolog
Gene Aliases: AW492986; BC002286; METTL27; WBSCR27
UniProt ID: (Human) Q8N6F8
Entrez Gene ID: (Human) 155368, (Mouse) 79565, (Rat) 688407
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