DGCR2
Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). The DGCR2 gene encodes the protein integral membrane protein DGCR2/IDD in humans.[1][2][3]
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.[3] DGCR2 is thought to interact with the Reelin complex to regulate corticogenesis.[4]
References
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Further reading
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External links
[edit | edit source]- DGCR2 human gene location in the UCSC Genome Browser.
- DGCR2 human gene details in the UCSC Genome Browser.
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