| 1 | IRF6, MACF1, RBM15, SETD2, TFAP2A, ZFHX3, ZFHX4
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| Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios
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| Bishop MR, Diaz Perez KK, Sun M, Ho S, Chopra P, Mukhopadhyay N, Hetmanski JB, Taub MA, Moreno-Uribe LM, Valencia-Ramirez LC, Restrepo Muñeton CP, Wehby G, Hecht JT, Deleyiannis F, Weinberg SM, Wu-Chou YH, Chen PK, Brand H, Epstein MP, Ruczinski I, Murray JC, Beaty TH, Feingold E, Lipinski RJ, Cutler DJ, Marazita ML, Leslie EJ
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| Am J Hum Genet. Jul 2;107(1):124-136. doi: 10.1016/j.ajhg.2020.05.018. Epub 2020 Jun 22. 2020
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| 2 | ZFHX4
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| Prognostic Role of Zinc Finger Homeobox 4 in Ovarian Serous Cystadenocarcinoma.
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| Ha M, Kim J, Park SM, Hong CM, Han ME, Song P, Kang CD, Lee D, Kim YH, Hur J, Oh SO.
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| Genet Test Mol Biomarkers. Mar;24(3):145-149. doi: 10.1089/gtmb.2019.0185. Epub 2020 Feb 27 2020
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| 3 | ZFHX4
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| Somatic mutations in ZFHX4 gene are associated with poor overall survival of Chinese esophageal squamous cell carcinoma patients.
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| Qing T, Zhu S, Suo C, Zhang L, Zheng Y, Shi L.
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| Sci Rep. Jul 10;7(1):4951. doi: 10.1038/s41598-017-04221-7 2017
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| 4 | CHD4, ZFHX4
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| ZFHX4 interacts with the NuRD core member CHD4 and regulates the glioblastoma tumor-initiating cell state.
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| Chudnovsky Y, Kim D, Zheng S, Whyte WA, Bansal M, Bray MA, Gopal S, Theisen MA, Bilodeau S, Thiru P, Muffat J, Yilmaz OH, Mitalipova M, Woolard K, Lee J, Nishimura R, Sakata N, Fine HA, Carpenter AE, Silver SJ, Verhaak RG, Califano A, Young RA, Ligon KL, Mellinghoff IK, Root DE, Sabatini DM, Hahn WC, Chheda MG.
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| Cell Rep. Jan 30;6(2):313-24. doi: 10.1016/j.celrep.2013.12.032. Epub 2014 Jan 16 2014
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| 5 | DEL8Q21, ZFHX4
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| Characterization of a 8q21.11 microdeletion syndrome associated with intellectual disability and a recognizable phenotype.
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| Palomares M, Delicado A, Mansilla E, de Torres ML, Vallespín E, Fernandez L, Martinez-Glez V, García-Miñaur S, Nevado J, Simarro FS, Ruiz-Perez VL, Lynch SA, Sharkey FH, Thuresson AC, Annerén G, Belligni EF, Martínez-Fernández ML, Bermejo E, Nowakowska B, Kutkowska-Kazmierczak A, Bocian E, Obersztyn E, Martínez-Frías ML, Hennekam RC, Lapunzina P.
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| Am J Hum Genet 89(2):295-301. Epub 2011 Jul 28.
2011
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| 6 | ZFHX4, PTOS1, PTOS2
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| Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family.
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| Nakashima M, Nakano M, Hirano A, Kishino T, Kondoh S, Miwa N, Niikawa N, Yoshiura K.
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| J Hum Genet 53(1):34-41. Epub 2007 Nov 7. 2008
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| 7 | ZFHX4
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| A homeodomain-zinc finger protein, ZFHX4, is expressed in neuronal differentiation manner and suppressed in muscle differentiation manner.
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| Hemmi K, Ma D, Miura Y, Kawaguchi M, Sasahara M, Hashimoto-Tamaoki T, Tamaoki T, Sakata N, Tsuchiya K.
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| Biol Pharm Bull 29(9):1830-5. 2006
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| 8 | PTOS1, ZFHX4
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| A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.
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| McMullan TW, Crolla JA, Gregory SG, Carter NP, Cooper RA, Howell GR, Robinson DO.
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| Hum Genet 110(3):244-50. 2002
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| 9 | ZFHX4
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| Expression of zfh-4, a new member of the zinc finger-homeodomain family, in developing brain and muscle.
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| Kostich WA, Sanes JR.
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| Dev Dyn. Feb;202(2):145-52. doi: 10.1002/aja.1002020206 1995
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