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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| DGCR2-20-RE | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-OR | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-GO | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-GR | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : DGCR2
Gene Name : DiGeorge syndrome critical region gene 2
Chromosome : CHR 22: 191,224,53-190,362,81
Locus : 22q11.21
Alt. Genes : FEM1B
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