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The '''''DGCR2''''' [[gene]] encodes the [[protein]] '''integral membrane protein DGCR2/IDD''' in humans.<ref name="pmid7655455">{{cite journal | vauthors = Wadey R, Daw S, Taylor C, Atif U, Kamath S, Halford S, O'Donnell H, Wilson D, Goodship J, Burn J | title = Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome | journal = Hum Mol Genet | volume = 4 | issue = 6 | pages = 1027–1033 | date = Oct 1995 | pmid = 7655455 | doi = 10.1093/hmg/4.6.1027 }}</ref><ref name="pmid8630060">{{cite journal | vauthors = Kajiwara K, Nagasawa H, Shimizu-Nishikawa K, Ookura T, Kimura M, Sugaya E | title = Cloning of SEZ-12 encoding seizure-related and membrane-bound adhesion protein | journal = Biochem Biophys Res Commun | volume = 222 | issue = 1 | pages = 144–148 | date = Jun 1996 | pmid = 8630060 | pmc =  | doi = 10.1006/bbrc.1996.0712 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: DGCR2 DiGeorge syndrome critical region gene 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9993| accessdate = }}</ref>
The '''''DGCR2''''' [[gene]] encodes the [[protein]] '''integral membrane protein DGCR2/IDD''' in humans.<ref name="pmid7655455">{{cite journal | vauthors = Wadey R, Daw S, Taylor C, Atif U, Kamath S, Halford S, O'Donnell H, Wilson D, Goodship J, Burn J | title = Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome | journal = Hum Mol Genet | volume = 4 | issue = 6 | pages = 1027–1033 | date = Oct 1995 | pmid = 7655455 | doi = 10.1093/hmg/4.6.1027 }}</ref><ref name="pmid8630060">{{cite journal | vauthors = Kajiwara K, Nagasawa H, Shimizu-Nishikawa K, Ookura T, Kimura M, Sugaya E | title = Cloning of SEZ-12 encoding seizure-related and membrane-bound adhesion protein | journal = Biochem Biophys Res Commun | volume = 222 | issue = 1 | pages = 144–148 | date = Jun 1996 | pmid = 8630060 | pmc =  | doi = 10.1006/bbrc.1996.0712 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: DGCR2 DiGeorge syndrome critical region gene 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9993| accessdate = }}</ref>

Latest revision as of 12:27, 9 January 2019

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Identifiers
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External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Wikidata
View/Edit Human

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]

References

  1. ↑ Wadey R, Daw S, Taylor C, Atif U, Kamath S, Halford S, O'Donnell H, Wilson D, Goodship J, Burn J (Oct 1995). "Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome". Hum Mol Genet. 4 (6): 1027–1033. doi:10.1093/hmg/4.6.1027. PMID 7655455.
  2. ↑ Kajiwara K, Nagasawa H, Shimizu-Nishikawa K, Ookura T, Kimura M, Sugaya E (Jun 1996). "Cloning of SEZ-12 encoding seizure-related and membrane-bound adhesion protein". Biochem Biophys Res Commun. 222 (1): 144–148. doi:10.1006/bbrc.1996.0712. PMID 8630060.
  3. ↑ 3.0 3.1 "Entrez Gene: DGCR2 DiGeorge syndrome critical region gene 2".

Further reading

  • Demczuk S, Aledo R, Zucman J, Delattre O, Desmaze C, Dauphinot L, Jalbert P, Rouleau GA, Thomas G, Aurias A (1995). "Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity". Hum. Mol. Genet. 4 (4): 551–558. doi:10.1093/hmg/4.4.551. PMID 7633403.
  • Nagase T, Seki N, Ishikawa K, Tanaka A, Nomura N (1996). "Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1". DNA Res. 3 (1): 17–24. doi:10.1093/dnares/3.1.17. PMID 8724849.
  • Gong W, Emanuel BS, Collins J, Kim DH, Wang Z, Chen F, Zhang G, Roe B, Budarf ML (1996). "A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11". Hum. Mol. Genet. 5 (6): 789–800. doi:10.1093/hmg/5.6.789. PMID 8776594.
  • Colland F, Jacq X, Trouplin V, Mougin C, Groizeleau C, Hamburger A, Meil A, Wojcik J, Legrain P, Gauthier JM (2004). "Functional proteomics mapping of a human signaling pathway". Genome Res. 14 (7): 1324–1332. doi:10.1101/gr.2334104. PMC 442148. PMID 15231748.
  • Collins JE, Wright CL, Edwards CA, Davis MP, Grinham JA, Cole CG, Goward ME, Aguado B, Mallya M, Mokrab Y, Huckle EJ, Beare DM, Dunham I (2005). "A genome annotation-driven approach to cloning the human ORFeome". Genome Biol. 5 (10): R84. doi:10.1186/gb-2004-5-10-r84. PMC 545604. PMID 15461802.
  • Shifman S, Levit A, Chen ML, Chen CH, Bronstein M, Weizman A, Yakir B, Navon R, Darvasi A (2007). "A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia". Hum. Genet. 120 (2): 160–170. doi:10.1007/s00439-006-0195-0. PMID 16783572.
  • Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–648. doi:10.1016/j.cell.2006.09.026. PMID 17081983.

External links


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