Human DGCR2 (NP_005128) VersaClone cDNA

R&D Systems | Catalog # RDC2514

R&D Systems
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Key Product Details

Species

Human

Accession Number

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Background: DGCR2

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. [provided by RefSeq]

Long Name

DiGeorge Syndrome Critical Region Gene 2

Alternate Names

KIAA0163, SEZ-12

Entrez Gene IDs

9993 (Human); 13356 (Mouse); 360742 (Rat)

Gene Symbol

DGCR2

UniProt

Additional DGCR2 Products

Product Documents for Human DGCR2 (NP_005128) VersaClone cDNA

Certificate of Analysis

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Product Specific Notices for Human DGCR2 (NP_005128) VersaClone cDNA

For research use only

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