ADAP2

{{Short description|Protein-coding gene in the species Homo sapiens}}

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Arf-GAP with dual PH domain-containing protein 2 is a protein that in humans is encoded by the ADAP2 gene.{{cite web | title = ADAP2 ArfGAP with dual PH domains 2 [ Homo sapiens (human) ]| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55803| accessdate = }}

References

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Further reading

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  • {{cite journal | vauthors=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1–2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 }}
  • {{cite journal | author=Suzuki Y |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library |journal=Gene |volume=200 |issue= 1–2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 | author2=Yoshitomo-Nakagawa K | author3=Maruyama K | display-authors=3 | last4=Suyama | first4=A | last5=Sugano | first5=S }}
  • {{cite journal | author=Jenne DE |title=A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions |journal=Genomics |volume=66 |issue= 1 |pages= 93–7 |year= 2000 |pmid= 10843809 |doi= 10.1006/geno.2000.6179 | author2=Tinschert S | author3=Stegmann E | display-authors=3 | last4=Reimann | first4=Heike | last5=Nürnberg | first5=Peter | last6=Horn | first6=Denise | last7=Naumann | first7=Ilka | last8=Buske | first8=Annegret | last9=Thiel | first9=Gundula }}
  • {{cite journal | author=Whitley P |title=Identification of centaurin-alpha2: a phosphatidylinositide-binding protein present in fat, heart and skeletal muscle |journal=Eur. J. Cell Biol. |volume=81 |issue= 4 |pages= 222–30 |year= 2003 |pmid= 12018390 |doi=10.1078/0171-9335-00242 | author2=Gibbard AM | author3=Koumanov F | display-authors=3 | last4=Oldfield | first4=S | last5=Kilgour | first5=EE | last6=Prestwich | first6=GD | last7=Holman | first7=GD }}
  • {{cite journal | author=Strausberg RL |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 | author2=Feingold EA | author3=Grouse LH | display-authors=3 | last4=Derge | first4=JG | last5=Klausner | first5=RD | last6=Collins | first6=FS | last7=Wagner | first7=L | last8=Shenmen | first8=CM | last9=Schuler | first9=GD |bibcode=2002PNAS...9916899M |doi-access=free }}
  • {{cite journal | vauthors=Hanck T, Stricker R, Sedehizade F, Reiser G |title=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 |journal=J. Neurochem. |volume=88 |issue= 2 |pages= 326–36 |year= 2004 |pmid= 14690521 |doi=10.1046/j.1471-4159.2003.02143.x |doi-access= |s2cid=19363530 }}
  • {{cite journal | author=Gerhard DS |title=The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC) |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 | author2=Wagner L | author3=Feingold EA | display-authors=3 | last4=Shenmen | first4=CM | last5=Grouse | first5=LH | last6=Schuler | first6=G | last7=Klein | first7=SL | last8=Old | first8=S | last9=Rasooly | first9=R }}
  • {{cite journal | author=Venturin M |title=Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval |journal=Ann. Hum. Genet. |volume=69 |issue= Pt 5 |pages= 508–16 |year= 2005 |pmid= 16138909 |doi= 10.1111/j.1529-8817.2005.00203.x | author2=Bentivegna A | author3=Moroni R | display-authors=3 | last4=Larizza | first4=L. | last5=Riva | first5=P. |s2cid=45891228 }}
  • {{cite journal | author=Douglas J |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963–5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083 | author2=Cilliers D | author3=Coleman K | display-authors=3 | last4=Tatton-Brown | first4=Katrina | last5=Barker | first5=Karen | last6=Bernhard | first6=Brigitte | last7=Burn | first7=John | last8=Huson | first8=Susan | last9=Josifova | first9=Dragana |s2cid=35797973 }}

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