| 1 | DDDFD, MN1, PBX1, PKNOX1, ZBTB24
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| Gain-of-Function MN1 Truncation Variants Cause a Recognizable Syndrome with Craniofacial and Brain Abnormalities.
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| Miyake N, Takahashi H, Nakamura K, Isidor B, Hiraki Y, Koshimizu E, Shiina M, Sasaki K, Suzuki H, Abe R, Kimura Y, Akiyama T, Tomizawa SI, Hirose T, Hamanaka K, Miyatake S, Mitsuhashi S, Mizuguchi T, Takata A, Obo K, Kato M, Ogata K, Matsumoto N.
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| Am J Hum Genet 106(1):13-25. doi: 10.1016/j.ajhg.2019.11.011. Epub 2019 Dec 12.
2020
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| 2 | DDDFD, MN1
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| MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis.
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| Mak CCY, Doherty D, Lin AE, Vegas N, Cho MT, Viot G, Dimartino C, Weisfeld-Adams JD, Lessel D, Joss S, Li C, Gonzaga-Jauregui C, Zarate YA, Ehmke N, Horn D, Troyer C, Kant SG, Lee Y, Ishak GE, Leung G, Barone Pritchard A, Yang S, Bend EG, Filippini F, Roadhouse C, Lebrun N, Mehaffey MG, Martin PM, Apple B, Millan F, Puk O, Hoffer MJV, Henderson LB, McGowan R, Wentzensen IM, Pei S, Zahir FR, Yu M, Gibson WT, Seman A, Steeves M, Murrell JR, Luettgen S, Francisco E, Strom TM, Amlie-Wolf L, Kaindl AM, Wilson WG, Halbach S, Basel-Salmon L, Lev-El N, Denecke J, Vissers LELM, Radtke K, Chelly J, Zackai E, Friedman JM, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics, Reid RR, Devriendt K, Chae JH, Stolerman E, McDougall C, Powis Z, Bienvenu T, Tan TY, Orenstein N, Dobyns WB, Shieh JT, Choi M, Waggoner D, Gripp KW, Parker MJ, Stoler J, Lyonnet S, Cormier-Daire V, Viskochil D, Hoffman TL, Amiel J, Chung BHY, Gordon CT.
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| Brain 143(1):55-68. doi: 10.1093/brain/awz379.
2020
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| 3 | MN1
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| High expression of meningioma 1 is correlated with reduced survival rates in colorectal cancer patients.
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| Ho YJ, Liu FC, Chang J, Shi B, Yeh KT, Lin YM, Lu JW.
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| Acta Histochem 121(5):628-637. doi: 10.1016/j.acthis.2019.05.006. Epub 2019 May 24.
2019
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| 4 | MEIS2, MN1
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| Meis2 as a critical player in MN1-induced leukemia.
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| Lai CK, Norddahl GL, Maetzig T, Rosten P, Lohr T, Sanchez Milde L, von Krosigk N, Docking TR, Heuser M, Karsan A, Humphries RK.
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| Blood Cancer J 7(9):e613. doi: 10.1038/bcj.2017.86.
2017
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| 5 | MN1
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| Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate.
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| Breckpot J, Anderlid BM, Alanay Y, Blyth M, Brahimi A, Duban-Bedu B, Gozé O, Firth H, Yakicier MC, Hens G, Rayyan M, Legius E, Vermeesch JR, Devriendt K.
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| Eur J Hum Genet 24(1):51-8. doi: 10.1038/ejhg.2015.65. Epub 2015 May 6.
2016
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| 6 | DDDFD, MN1
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| Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene.
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| Beck M, Peterson JF, McConnell J, McGuire M, Asato M, Losee JE, Surti U, Madan-Khetarpal S, Rajkovic A, Yatsenko SA.
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| Am J Med Genet A 167A(5):1047-53. doi: 10.1002/ajmg.a.36839. Epub 2015 Mar 21.
2015
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| 7 | MN1
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| Mapping of MN1 sequences necessary for myeloid transformation.
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| Kandilci A, Surtel J, Janke L, Neale G, Terranova S, Grosveld GC.
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| PLoS One 8(4):e61706. doi: 10.1371/journal.pone.0061706. Print 2013.
2013
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| 8 | ETV6, MN1
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| MN1-ETV6 fusion gene arising from MDS with 5q-.
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| Nofrini V, Berchicci L, La Starza R, Gorello P, Di Giacomo D, Arcioni F, Pierini V, Crescenzi B, Romoli S, Matteucci C, Mecucci C.
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| Leuk Res 35(7):e123-6. doi: 10.1016/j.leukres.2011.03.019. Epub 2011 May 19. No abstract available.
2011
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| 9 | MN1
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| Functional characterization of high levels of meningioma 1 as collaborating oncogene in acute leukemia.
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| Liu T, Jankovic D, Brault L, Ehret S, Baty F, Stavropoulou V, Rossi V, Biondi A, Schwaller J.
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| Leukemia 24(3):601-12. doi: 10.1038/leu.2009.272. Epub 2010 Jan 14.
2010
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| 10 | CEBPA, MN1
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| Reintroduction of CEBPA in MN1-overexpressing hematopoietic cells prevents their hyperproliferation and restores myeloid differentiation.
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| Kandilci A, Grosveld GC.
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| Blood 114(8):1596-606. Epub 2009 Jun 26.PMID: 19561324 2009
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| 11 | ADCY5, EFNA5, ERC2, GFPT2, GIPC2, GNA14, HSPA4L, MAGI1, MN1, MSX2, MYO5B, OCLN, RSPO1, SALL1, ZNF382
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| Genome-wide identification of aberrantly methylated promoter associated CpG islands in acute lymphocytic leukemia.
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| Kuang SQ, Tong WG, Yang H, Lin W, Lee MK, Fang ZH, Wei Y, Jelinek J, Issa JP, Garcia-Manero G.
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| Leukemia 22(8):1529-38. Epub 2008 Jun 5.PMID: 18528427 2008
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| 12 | IGFBP5, MN1
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| The MN1 oncoprotein activates transcription of the IGFBP5 promoter through a CACCC-rich consensus sequence.
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| Meester-Smoor MA, Molijn AC, Zhao Y, Groen NA, Groffen CA, Boogaard M, van Dalsum-Verbiest D, Grosveld GC, Zwarthoff EC.
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| J Mol Endocrinol 38(1-2):113-25.
2007
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| 13 | MN1
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| MN1, a novel player in human AML.
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| Grosveld GC.
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| Blood Cells Mol Dis 39(3):336-9. Epub 2007 Aug 14. Review.
2007
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| 14 | MN1
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| The MN1 oncoprotein synergizes with coactivators RAC3 and p300 in RAR-RXR-mediated transcription.
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| van Wely KH, Molijn AC, Buijs A, Meester-Smoor MA, Aarnoudse AJ, Hellemons A, den Besten P, Grosveld GC, Zwarthoff EC.
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| Oncogene 22(5):699-709.
2003
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| 15 | C22orf33, MN1, RABL4
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| A first-generation linkage disequilibrium map of human chromosome 22.
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| Dawson E, Abecasis GR, Bumpstead S, Chen Y, Hunt S, Beare DM, Pabial J, Dibling T, Tinsley E, Kirby S, Carter D, Papaspyridonos M, Livingstone S, Ganske R, Lohmussaar E, Zernant J, Tonisson N, Remm M, Magi R, Puurand T, Vilo J, Kurg A, Rice K, Deloukas P, Mott R, Metspalu A, Bentley DR, Cardon LR, Dunham I.
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| Nature 418(6897):544-8. 2002
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| 16 | ETV6, MN1
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| Translocation (12;22) (p13;q11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MN1 gene on 22q11.
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| Buijs A, et al.
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| Oncogene 10 : 1511-1519. 1995
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| 17 | MN1
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| Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma.
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| Lekanne Deprez RH, Riegman PH, Groen NA, Warringa UL, van Biezen NA, Molijn AC, Bootsma D, de Jong PJ, Menon AG, Kley NA, et al.
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| Oncogene 10(8):1521-8. 1995
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