| 1 | DDGRM, MORC2
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| De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism.
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| Guillen Sacoto MJ, Tchasovnikarova IA, Torti E, Forster C, Andrew EH, Anselm I, Baranano KW, Briere LC, Cohen JS, Craigen WJ, Cytrynbaum C, Ekhilevitch N, Elrick MJ, Fatemi A, Fraser JL, Gallagher RC, Guerin A, Haynes D, High FA, Inglese CN, Kiss C, Koenig MK, Krier J, Lindstrom K, Marble M, Meddaugh H, Moran ES, Morel CF, Mu W, Muller EA 2nd, Nance J, Natowicz MR, Numis AL, Ostrem B, Pappas J, Stafstrom CE, Streff H, Sweetser DA, Szybowska M; Undiagnosed Diseases Network, Walker MA, Wang W, Weiss K, Weksberg R, Wheeler PG, Yoon G, Kingston RE, Juusola J.
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| Am J Hum Genet. Aug 6;107(2):352-363. doi: 10.1016/j.ajhg.2020.06.013. Epub 2020 Jul 20. 2020
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| 2 | CTNND1, MORC2
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| Chromatin remodeling protein MORC2 promotes breast cancer invasion and metastasis through a PRD domain-mediated interaction with CTNND1.
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| Liao XH, Zhang Y, Dong WJ, Shao ZM, Li DQ.
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| Oncotarget ncotarget. 2017 Jun 16. doi: 10.18632/oncotarget.18556. [Epub ahead of print]
2017
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| 3 | MORC2
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| Hyperactivation of HUSH complex function by Charcot-Marie-Tooth disease mutation in MORC2.
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| Tchasovnikarova IA, Timms RT, Douse CH, Roberts RC, Dougan G, Kingston RE, Modis Y, Lehner PJ.
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| Nat Genet 49(7):1035-1044. doi: 10.1038/ng.3878. Epub 2017 Jun 5.
2017
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| 4 | CMT2Z, MORC2
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| MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.
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| Albulym OM, Kennerson ML, Harms MB, Drew AP, Siddell AH, Auer-Grumbach M, Pestronk A, Connolly A, Baloh RH, Zuchner S, Reddel SW, Nicholson GA.
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| Ann Neurol 79(3):419-27. doi: 10.1002/ana.24575. Epub 2016 Jan 13.
2016
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| 5 | CMT2Z, MORC2
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| Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.
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| Sevilla T, Lupo V, Martínez-Rubio D, Sancho P, Sivera R, Chumillas MJ, García-Romero M, Pascual-Pascual SI, Muelas N, Dopazo J, Vílchez JJ, Palau F, Espinós C.
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| Brain 139(Pt 1):62-72. doi: 10.1093/brain/awv311. Epub 2015 Oct 24.
2016
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| 6 | CMT2Z, MORC2
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| Clinico-genetics in Korean Charcot-Marie-Tooth disease type 2Z with MORC2 mutations.
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| Hyun YS, Hong YB, Choi BO, Chung KW.
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| Brain 139(Pt 7):e40. doi: 10.1093/brain/aww082. Epub 2016 Apr 21. No abstract available.
2016
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| 7 | EZH2, MORC2, SORBS2
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| Microchidia protein 2, MORC2, downregulates the cytoskeleton adapter protein, ArgBP2, via histone methylation in gastric cancer cells.
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| Tong Y, Li Y, Gu H, Wang C, Liu F, Shao Y, Li J, Cao L, Li F.
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| Biochem Biophys Res Commun 467(4):821-7. doi: 10.1016/j.bbrc.2015.10.059. Epub 2015 Oct 22.
2015
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| 8 | CDKN1A, MORC2
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| By recruiting HDAC1, MORC2 suppresses p21 Waf1/Cip1 in gastric cancer.
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| Zhang Q, Song Y, Chen W, Wang X, Miao Z, Cao L, Li F, Wang G.
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| Oncotarget 6(18):16461-70.
2015
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| 9 | ACLY, MORC2
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| Cytosolic functions of MORC2 in lipogenesis and adipogenesis.
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| Sánchez-Solana B, Li DQ, Kumar R.
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| Biochim Biophys Acta 1843(2):316-26. doi: 10.1016/j.bbamcr.2013.11.012. Epub 2013 Nov 25.
2014
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| 10 | MORC2, PAK1
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| MORC2 signaling integrates phosphorylation-dependent, ATPase-coupled chromatin remodeling during the DNA damage response.
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| Li DQ, Nair SS, Ohshiro K, Kumar A, Nair VS, Pakala SB, Reddy SD, Gajula RP, Eswaran J, Aravind L, Kumar R.
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| Cell Rep 2(6):1657-69. doi: 10.1016/j.celrep.2012.11.018.
2012
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| 11 | MORC2
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| Identification and expression analysis of a novel CW-type zinc finger protein MORC2 in cancer cells.
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| Wang GL, Wang CY, Cai XZ, Chen W, Wang XH, Li F.
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| Anat Rec (Hoboken) 293(6):1002-9. doi: 10.1002/ar.21119.
2010
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| 12 | ABLIM3, ABLIM3, ABLIM3, ADGRL1, ADNP2, AHCYL2, ANKRD12, AP2A1, AP2A2, ARHGEF15, C20orf117, CLSTN1, CNKSR2, DHX30, DMXL2, EEF1AKNMT, EHBP1, FAF2, FBXO4, GOLGA8A, IVNS1ABP, MCF2L2, MLXIP, MORC2, NUP210, PCF11, PCYOX1, PNMA2, RAB11FIP5, RASGRP3, RHOBTB3, RUFY3, SACM1L, SCFD1, SEC31A, SLCO2B1, SLITRK3, UBOX5, USP19, WDR47, WWC1, ZC3H13, ZHX2, ZNF365
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| Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
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| Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, TanakaA, Kotani H, Nomura N, Ohara O.
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| DNA Res 5(6):355-64. 1998
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