Lentiviral human DGCR2 sgRNA gene knockout kit

Human DGCR2

Gene symbol: DGCR2
Synonyms: DGS-C IDD LAN SEZ-12
Species: HUMAN
Gene ID: 9993
Summary: Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_005137:6:6 NM_001173533:5:5 NM_001173534:5:5 NM_001184781:6:6