| 1 | C14orf39, POF18, SPGF52, SYCE1
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| Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans
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| Fan S, Jiao Y, Khan R, Jiang X, Javed AR, Ali A, Zhang H, Zhou J, Naeem M, Murtaza G, Li Y, Yang G, Zaman Q, Zubair M, Guan H, Zhang X, Ma H, Jiang H, Ali H, Dil S, Shah W, Ahmad N, Zhang Y, Shi Q.
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| Am J Hum Genet. Feb 4;108(2):324-336. doi: 10.1016/j.ajhg.2021.01.010. Epub 2021 Jan 27 2021
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| 2 | C14orf39, SYCE1
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| Meiotic chromosome synapsis depends on multivalent SYCE1-SIX6OS1 interactions that are disrupted in cases of human infertility
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| Sánchez-Sáez F, Gómez-H L, Dunne OM, Gallego-Páramo C, Felipe-Medina N, Sánchez-Martín M, Llano E, Pendas AM, Davies OR
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| Sci Adv. Sep 2;6(36):eabb1660. doi: 10.1126/sciadv.abb1660. 2020
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| 3 | SPGF15, SYCE1
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| The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.
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| Pashaei M, Rahimi Bidgoli MM, Zare-Abdollahi D, Najmabadi H, Haji-Seyed-Javadi R, Fatehi F, Alavi A.
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| J Assist Reprod Genet. Feb;37(2):451-458. doi: 10.1007/s10815-019-01660-1. Epub 2020 Jan 8. 2020
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| 4 | C14Orf39, SYCE1, SYCE2, TEX12
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| Molecular structure of human synaptonemal complex protein SYCE1.
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| Dunne OM, Davies OR.
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| Chromosoma. Sep;128(3):223-236. doi: 10.1007/s00412-018-00688-z. Epub 2019 Jan 3 2019
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| 5 | C14orf39, SYCE1, SYCE3, SYCP1, SYCP3
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| A molecular model for self-assembly of the synaptonemal complex protein SYCE3.
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| Dunne OM, Davies OR.
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| J Biol Chem. Jun 7;294(23):9260-9275. doi: 10.1074/jbc.RA119.008404. Epub 2019 Apr 25. 2019
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| 6 | C14orf39, SYCE1
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| C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility
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| Gómez-H L, Felipe-Medina N, Sánchez-Martín M, Davies OR, Ramos I, García-Tuñón I, de Rooij DG, Dereli I, Tóth A, Barbero JL, Benavente R, Llano E, Pendas AM.
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| Nat Commun. Oct 31;7:13298. doi: 10.1038/ncomms13298. 2016
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| 7 | SPGF15, SYCE1
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| Mutations in Genes Coding for Synaptonemal Complex Proteins and Their Impact on Human Fertility
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| Geisinger A, Benavente R.
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| Cytogenet Genome Res. 150(2):77-85. doi: 10.1159/000453344. Epub 2016 Dec 21 2016
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| 8 | SPGF15, SYCE1
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| Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia.
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| Maor-Sagie E, Cinnamon Y, Yaacov B, Shaag A, Goldsmidt H, Zenvirt S, Laufer N, Richler C, Frumkin A.
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| J Assist Reprod Genet. Jun;32(6):887-91. doi: 10.1007/s10815-015-0445-y. Epub 2015 Apr 22. 2015
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| 9 | SYCE1, SYCE3
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| Structural insight into the central element assembly of the synaptonemal complex.
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| Lu J, Gu Y, Feng J, Zhou W, Yang X, Shen Y.
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| Sci Rep. Nov 14;4:7059. doi: 10.1038/srep07059 2014
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| 10 | POF12, SYCE1
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| Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency
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| de Vries L, Behar DM, Smirin-Yosef P, Lagovsky I, Tzur S, Basel-Vanagaite L.
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| J Clin Endocrinol Metab. Oct;99(10):E2129-32. doi: 10.1210/jc.2014-1268. Epub 2014 Jul 25. 2014
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| 11 | SYCE1, SYCE2
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| Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair.
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| Bolcun-Filas E, Speed R, Taggart M, Grey C, de Massy B, Benavente R, Cooke HJ.
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| PLoS Genet 5(2):e1000393. Epub 2009 Feb 27.
2009
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| 12 | SCYP1, SYCE1, SYCE2
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| SYCE2 is required for synaptonemal complex assembly, double strand break repair, and homologous recombination.
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| Bolcun-Filas E, Costa Y, Speed R, Taggart M, Benavente R, De Rooij DG, Cooke HJ.
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| J Cell Biol 176(6):741-7. Epub 2007 Mar 5.
2007
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| 13 | SYCE1, SYCE2, SYCP1, TEX12
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| Characterization of a novel meiosis-specific protein within the central element of the synaptonemal complex.
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| Hamer G, Gell K, Kouznetsova A, Novak I, Benavente R, Höög C.
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| J Cell Sci 119(Pt 19):4025-32. Epub 2006 Sep 12.
2006
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| 14 | SYCE1, SYCE2, SYCP1
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| Two novel proteins recruited by synaptonemal complex protein 1 (SYCP1) are at the centre of meiosis.
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| Costa Y, Speed R, Ollinger R, Alsheimer M, Semple CA, Gautier P, Maratou K, Novak I, Hoog C, Benavente R, Cooke HJ.
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| J Cell Sci 118(Pt 12):2755-62. 2005
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| 15 | SYCE1
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| Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin.
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| van Geel M, Dickson MC, Beck AF, Bolland DJ, Frants RR, van der Maarel SM, de Jong PJ, Hewitt JE.
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| Genomics 79(2):210-7. 2002
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