Citations for
1FZR1, IDH2
APC/C CDH1 ubiquitinates IDH2 contributing to ROS increase in mitosis.
Lambhate S, Bhattacharjee D, Jain N.
Cell Signal. Oct;86:110087. doi: 10.1016/j.cellsig.2021.110087. Epub 2021 Jul 13. 2021
2IDH2, INTS3, SRSF2
Coordinated alterations in RNA splicing and epigenetic regulation drive leukaemogenesis.
Yoshimi A, Lin KT, Wiseman DH, Rahman MA, Pastore A, Wang B, Lee SC, Micol JB, Zhang XJ, de Botton S, Penard-Lacronique V, Stein EM, Cho H, Miles RE, Inoue D, Albrecht TR, Somervaille TCP, Batta K, Amaral F, Simeoni F, Wilks DP, Cargo C, Intlekofer AM, Levine RL, Dvinge H, Bradley RK, Wagner EJ, Krainer AR, Abdel-Wahab O.
Nature Oct;574(7777):273-277. doi: 10.1038/s41586-019-1618-0. Epub 2019 Oct 2 2019
3G6PD, IDH2, SIRT5
SIRT5 promotes IDH2 desuccinylation and G6PD deglutarylation to enhance cellular antioxidant defense.
Zhou L, Wang F, Sun R, Chen X, Zhang M, Xu Q, Wang Y, Wang S, Xiong Y, Guan KL, Yang P, Yu H, Ye D.
EMBO Rep 17(6):811-22. doi: 10.15252/embr.201541643. Epub 2016 Apr 9. 2016
4IDH1, IDH2
Isocitrate dehydrogenase mutation is frequently observed in giant cell tumor of bone.
Kato Kaneko M, Liu X, Oki H, Ogasawara S, Nakamura T, Saidoh N, Tsujimoto Y, Matsuyama Y, Uruno A, Sugawara M, Tsuchiya T, Yamakawa M, Yamamoto M, Takagi M, Kato Y.
Cancer Sci 105(6):744-8. doi: 10.1111/cas.12413. 2014
5COL2A1, IDH1, IDH2
Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.
Tarpey PS, Behjati S, Cooke SL, Van Loo P, Wedge DC, Pillay N, Marshall J, O'Meara S, Davies H, Nik-Zainal S, Beare D, Butler A, Gamble J, Hardy C, Hinton J, Jia MM, Jayakumar A, Jones D, Latimer C, Maddison M, Martin S, McLaren S, Menzies A, Mudie L, Raine K, Teague JW, Tubio JM, Halai D, Tirabosco R, Amary F, Campbell PJ, Stratton MR, Flanagan AM, Futreal PA.
Nat Genet 45(8):923-6. doi: 10.1038/ng.2668. Epub 2013 Jun 16. 2013
6IDH1, IDH2
IDH mutations in tumorigenesis and their potential role as novel therapeutic targets.
Krell D, Mulholland P, Frampton AE, Krell J, Stebbing J, Bardella C.
Future Oncol 9(12):1923-35. doi: 10.2217/fon.13.143. Review. 2013
7IDH1, IDH2
IDH mutation impairs histone demethylation and results in a block to cell differentiation.
Lu C, Ward PS, Kapoor GS, Rohle D, Turcan S, Abdel-Wahab O, Edwards CR, Khanin R, Figueroa ME, Melnick A, Wellen KE, O'Rourke DM, Berger SL, Chan TA, Levine RL, Mellinghoff IK, Thompson CB.
Nature 483(7390):474-8. doi: 10.1038/nature10860. 2012
8IDH2, SIRT3
SIRT3 protein deacetylates isocitrate dehydrogenase 2 (IDH2) and regulates mitochondrial redox status.
Yu W, Dittenhafer-Reed KE, Denu JM.
J Biol Chem 287(17):14078-86. doi: 10.1074/jbc.M112.355206. Epub 2012 Mar 13. 2012
9D2HA, D2HGDH, IDH1, IDH2
IDH1 and IDH2 have critical roles in 2-hydroxyglutarate production in D-2-hydroxyglutarate dehydrogenase depleted cells.
Matsunaga H, Futakuchi-Tsuchida A, Takahashi M, Ishikawa T, Tsuji M, Ando O.
Biochem Biophys Res Commun 423(3):553-6. doi: 10.1016/j.bbrc.2012.06.002. Epub 2012 Jun 7. 2012
10ECDMM3, ECDMM4, IDH1, IDH2
Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.
Pansuriya TC, van Eijk R, d'Adamo P, van Ruler MA, Kuijjer ML, Oosting J, Cleton-Jansen AM, van Oosterwijk JG, Verbeke SL, Meijer D, van Wezel T, Nord KH, Sangiorgi L, Toker B, Liegl-Atzwanger B, San-Julian M, Sciot R, Limaye N, Kindblom LG, Daugaard S, Godfraind C, Boon LM, Vikkula M, Kurek KC, Szuhai K, French PJ, Bovée JV.
Nat Genet 43(12):1256-61. doi: 10.1038/ng.1004. 2011
11IDH1, IDH2
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.
Amary MF, Damato S, Halai D, Eskandarpour M, Berisha F, Bonar F, McCarthy S, Fantin VR, Straley KS, Lobo S, Aston W, Green CL, Gale RE, Tirabosco R, Futreal A, Campbell P, Presneau N, Flanagan AM.
Nat Genet 43(12):1262-5. doi: 10.1038/ng.994. 2011
12IDH2
Hypoxia promotes isocitrate dehydrogenase-dependent carboxylation of α-ketoglutarate to citrate to support cell growth and viability.
Wise DR, Ward PS, Shay JE, Cross JR, Gruber JJ, Sachdeva UM, Platt JM, DeMatteo RG, Simon MC, Thompson CB.
Proc Natl Acad Sci U S A 108(49):19611-6. doi: 10.1073/pnas.1117773108. Epub 2011 Nov 21. 2011
13IDH1, IDH2
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.
Amary MF, Damato S, Halai D, Eskandarpour M, Berisha F, Bonar F, McCarthy S, Fantin VR, Straley KS, Lobo S, Aston W, Green CL, Gale RE, Tirabosco R, Futreal A, Campbell P, Presneau N, Flanagan AM.
Nat Genet 43(12):1262-5. doi: 10.1038/ng.994. 2011
14D2HA2, IDH2
IDH2 mutations in patients with D-2-hydroxyglutaric aciduria.
Kranendijk M, Struys EA, van Schaftingen E, Gibson KM, Kanhai WA, van der Knaap MS, Amiel J, Buist NR, Das AM, de Klerk JB, Feigenbaum AS, Grange DK, Hofstede FC, Holme E, Kirk EP, Korman SH, Morava E, Morris A, Smeitink J, Sukhai RN, Vallance H, Jakobs C, Salomons GS.
Science 330(6002):336. Epub 2010 Sep 16. 2010
15IDH1, IDH2
IDH1 or IDH2 mutations predict longer survival and response to temozolomide in low-grade gliomas.
Houillier C, Wang X, Kaloshi G, Mokhtari K, Guillevin R, Laffaire J, Paris S, Boisselier B, Idbaih A, Laigle-Donadey F, Hoang-Xuan K, Sanson M, Delattre JY.
Neurology 75(17):1560-6. 2010
16IDH1, IDH2
Glioma-derived mutations in IDH: from mechanism to potential therapy.
Fu Y, Huang R, Du J, Yang R, An N, Liang A.
Biochem Biophys Res Commun 397(2):127-30. Epub 2010 May 27. Review. 2010
17IDH1, IDH2
Acquired mutations in the genes encoding IDH1 and IDH2 both are recurrent aberrations in acute myeloid leukemia: prevalence and prognostic value.
Abbas S, Lugthart S, Kavelaars FG, Schelen A, Koenders JE, Zeilemaker A, van Putten WJ, Rijneveld AW, Löwenberg B, Valk PJ.
Blood 116(12):2122-6. Epub 2010 Jun 10. 2010
18IDH1, IDH2
The common feature of leukemia-associated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate.
Ward PS, Patel J, Wise DR, Abdel-Wahab O, Bennett BD, Coller HA, Cross JR, Fantin VR, Hedvat CV, Perl AE, Rabinowitz JD, Carroll M, Su SM, Sharp KA, Levine RL, Thompson CB.
Cancer Cell 17(3):225-34. Epub 2010 Feb 18.PMID: 20171147 2010
19IDH2, SIRT3
Sirt3 mediates reduction of oxidative damage and prevention of age-related hearing loss under caloric restriction.
Someya S, Yu W, Hallows WC, Xu J, Vann JM, Leeuwenburgh C, Tanokura M, Denu JM, Prolla TA.
Cell 143(5):802-12. 2010
20IDH1, IDH2
Diagnostic use of IDH1/2 mutation analysis in routine clinical testing of formalin-fixed, paraffin-embedded glioma tissues.
Horbinski C, Kofler J, Kelly LM, Murdoch GH, Nikiforova MN.
J Neuropathol Exp Neurol 68(12):1319-25. 2009
21IDH1, IDH2
IDH1 and IDH2 mutations in gliomas.
Yan H, Parsons DW, Jin G, McLendon R, Rasheed BA, Yuan W, Kos I, Batinic-Haberle I, Jones S, Riggins GJ, Friedman H, Friedman A, Reardon D, Herndon J, Kinzler KW, Velculescu VE, Vogelstein B, Bigner DD.
N Engl J Med 360(8):765-73.PMID: 19228619 2009
22IDH1, IDH2
Novel allosteric properties produced by residue substitutions in the subunit interface of yeast NAD+-specific isocitrate dehydrogenase.
Hu G, McAlister-Henn L.
Arch Biochem Biophys 453(2):207-16. Epub 2006 Jul 12.PMID: 16884682 2006
23IDH1, IDH2
Physiological consequences of loss of allosteric activation of yeast NAD+-specific isocitrate dehydrogenase.
Hu G, Lin AP, McAlister-Henn L.
J Biol Chem 281(25):16935-42. Epub 2006 Apr 18.PMID: 16621803 2006
24IDH2, IDH3A
Assignment of the human mitochondrial NADP+-specific isocitrate dehydrogenase (IDH2) gene to 15q26.1 by in situ hybridization.
Oh IU, et al.
Genomics 38 : 104-106. 1996
25IDH2
Cloning of a cDNA encoding bovine mitochondrial NADP+-specific isocitrate dehydrogenase and structural comparison with its isoenzymes from different species.
Huh TL, et al.
Biochem J 292 : 705-710. 1993
26IDH2, MAN2C1, MPI, PKM
Assignment of cytoplasmic alpha-mannosidase (MANN-A) and confirmation of mitochondrial isocitrate dehydrogenase (IDH-M) to the q11-qter region of chromosome 15 in man.
Champion MJ, et al.
Cytogenet Cell Genet 22 : 498-502. 1978
27IDH2
Human mitochondrial NADP-dependent isocitrate dehydrogenase in man-mouse somatic cell hybrids.
Bruns GAP, et al.
Cytogenet Cell Genet 17 : 200-211. 1976
28IDH2
Assignment of a gene for human mitochondrial isocitrate dehydrogenase (ICD-M, EC 1.1.1.41) to chromosome 15.
Grzeschik KH.
Hum Genet 34 : 23-28. 1976
29AK1, ENO2, GUSB, IDH2
Assignment of human genes: beta-glucuronidase to chromosome 7, adenylate kinase-1 to 9, a second enzyme with enolase activity to 12, and mitochondrial IDH to 15.
Grzeschik KH.
Cytogenet Cell Genet 16 : 142-148. 1976