CENTA2 explained

Arf-GAP with dual PH domain-containing protein 2 is a protein that in humans is encoded by the ADAP2 gene.^[1]

Further reading

• Maruyama K, Sugano S . Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. . Gene . 138 . 1–2 . 171–4 . 1994 . 8125298 . 10.1016/0378-1119(94)90802-8 .
• Suzuki Y . Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library . Gene . 200 . 1–2 . 149–56 . 1997 . 9373149 . 10.1016/S0378-1119(97)00411-3 . Yoshitomo-Nakagawa K . Maruyama K . 3 . Suyama . A . Sugano . S .
• Jenne DE . A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions . Genomics . 66 . 1 . 93–7 . 2000 . 10843809 . 10.1006/geno.2000.6179 . Tinschert S . Stegmann E . 3 . Reimann . Heike . Nürnberg . Peter . Horn . Denise . Naumann . Ilka . Buske . Annegret . Thiel . Gundula .
• Whitley P . Identification of centaurin-alpha2: a phosphatidylinositide-binding protein present in fat, heart and skeletal muscle . Eur. J. Cell Biol. . 81 . 4 . 222–30 . 2003 . 12018390 . 10.1078/0171-9335-00242 . Gibbard AM . Koumanov F . 3 . Oldfield . S . Kilgour . EE . Prestwich . GD . Holman . GD .
• Strausberg RL . Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences . Proc. Natl. Acad. Sci. U.S.A. . 99 . 26 . 16899–903 . 2003 . 12477932 . 10.1073/pnas.242603899 . 139241 . Feingold EA . Grouse LH . 3 . Derge . JG . Klausner . RD . Collins . FS . Wagner . L . Shenmen . CM . Schuler . GD . 2002PNAS...9916899M . free .
• Hanck T, Stricker R, Sedehizade F, Reiser G . Identification of gene structure and subcellular localization of human centaurin alpha 2, and p42IP4, a family of two highly homologous, Ins 1,3,4,5-P4-/PtdIns 3,4,5-P3-binding, adapter proteins . J. Neurochem. . 88 . 2 . 326–36 . 2004 . 14690521 . 10.1046/j.1471-4159.2003.02143.x . 19363530 .
• Gerhard DS . The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC) . Genome Res. . 14 . 10B . 2121–7 . 2004 . 15489334 . 10.1101/gr.2596504 . 528928 . Wagner L . Feingold EA . 3 . Shenmen . CM . Grouse . LH . Schuler . G . Klein . SL . Old . S . Rasooly . R .
• Venturin M . Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval . Ann. Hum. Genet. . 69 . Pt 5 . 508–16 . 2005 . 16138909 . 10.1111/j.1529-8817.2005.00203.x . Bentivegna A . Moroni R . 3 . Larizza . L. . Riva . P. . 45891228 .
• Douglas J . Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth . Nat. Genet. . 39 . 8 . 963–5 . 2007 . 17632510 . 10.1038/ng2083 . Cilliers D . Coleman K . 3 . Tatton-Brown . Katrina . Barker . Karen . Bernhard . Brigitte . Burn . John . Huson . Susan . Josifova . Dragana . 35797973 .

Notes and References

1. Web site: Entrez Gene: CENTA2 centaurin, alpha 2.