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WBSCR27


Official Full Name
methyltransferase like 27
Organism
Homo sapiens
Gene ID
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

Cat.No. Product Name Price
SHH445800 shRNA set against Human WBSCR27 (NM_152559.2) Inquiry
SHH445804 shRNA set against Mouse WBSCR27 (NM_024479.2) Inquiry
SHH445808 shRNA set against Rat WBSCR27 (NM_001109499.2) Inquiry
SHL130332 shRNA set against Human WBSCR27(NM_152559.2) Inquiry
SHL130368 shRNA set against Mouse Wbscr27(NM_024479.2) Inquiry
SHW009685 shRNA set against Danio rerio WBSCR27 (NM_001040381) Inquiry
Cat.No. Product Name Price
CDFG009617 Human WBSCR27 cDNA Clone(NM_152559.2) Inquiry
CDFR009033 Rat Wbscr27 cDNA Clone(NM_001109499.2) Inquiry
MiUTR1H-11196 WBSCR27 miRNA 3'UTR clone Inquiry
MiUTR1M-12739 WBSCR27 miRNA 3'UTR clone Inquiry
CDCB171160 Danio rerio WBSCR27 ORF Clone (NM_001040381) Inquiry
CDCB191027 Rabbit WBSCR27 ORF clone (XM_008249089.1) Inquiry
CDCH100628 human WBSCR27 ORF clone (NM_152559.2) Inquiry
CDCH100632 Mouse Wbscr27 ORF clone (NM_024479.2) Inquiry
CDCR376070 Rat Wbscr27 ORF Clone(NM_001109499.2) Inquiry
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