Lentiviral human ESS2 sgRNA gene knockout kit

Human ESS2

Gene symbol: ESS2
Synonyms: bis1 DGCR13 DGCR14 DGS-H DGS-I DGSH DGSI ES2 Es2el ESS-2
Species: HUMAN
Gene ID: 8220
Summary: This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_022719:4:4