Citations for
1BRPF1, KAT6A, KAT6B, KAT7
BRPF1 is essential for development of fetal hematopoietic stem cells.
You L, Li L, Zou J, Yan K, Belle J, Nijnik A, Wang E, Yang XJ.
J Clin Invest 126(9):3247-62. doi: 10.1172/JCI80711. 2016
2KAT6B, MYO1C
Molecular motor MYO1C, acetyltransferase KAT6B and osteogenetic transcription factor RUNX2 expression in human masseter muscle contributes to development of malocclusion.
Desh H, Gray SL, Horton MJ, Raoul G, Rowlerson AM, Ferri J, Vieira AR, Sciote JJ.
Arch Oral Biol 59(6):601-7. doi: 10.1016/j.archoralbio.2014.03.005. Epub 2014 Mar 20. 2014
3KAT6B, OHDO
Further delineation of the KAT6B molecular and phenotypic spectrum.
Gannon T, Perveen R, Schlecht H, Ramsden S, Anderson B, Kerr B, Day R, Banka S, Suri M, Berland S, Gabbett M, Ma A, Lyonnet S, Cormier-Daire V, Yilmaz R, Borck G, Wieczorek D, Anderlid BM, Smithson S, Vogt J, Moore-Barton H, Simsek-Kiper PO, Maystadt I, Destrée A, Bucher J, Angle B, Mohammed S, Wakeling E, Price S, Singer A, Sznajer Y, Toutain A, Haye D, Newbury-Ecob R, Fradin M, McGaughran J, Tuysuz B, Tein M, Bouman K, Dabir T, Van den Ende J, Luk HM, Pilz DT, Eason J, Davies S, Reardon W, Garavelli L, Zuffardi O, Devriendt K, Armstrong R, Johnson D, Doco-Fenzy M, Bijlsma E, Unger S, Veenstra-Knol HE, Kohlhase J, Lo IF; DDD study, Smith J, Clayton-Smith J.
Eur J Hum Genet ur J Hum Genet. 2014 Nov 26. doi: 10.1038/ejhg.2014.248. [Epub ahead of print] 2014
4KAT6B, OHDO
An individual with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and additional features expands the phenotype associated with mutations in KAT6B.
Yu HC, Geiger EA, Medne L, Zackai EH, Shaikh TH.
Am J Med Genet A 164A(4):950-7. doi: 10.1002/ajmg.a.36379. Epub 2014 Jan 23. 2014
5KAT6B, OHDO
De novo mutations of the gene encoding the histone acetyltransferase KAT6B in two patients with Say-Barber/Biesecker/Young-Simpson syndrome.
Szakszon K, Salpietro C, Kakar N, Knegt AC, Oláh E, Dallapiccola B, Borck G.
Am J Med Genet A m J Med Genet A. 2013 Feb 22. doi: 10.1002/ajmg.a.35848. [Epub ahead of print] 2013
6GPATS, KAT6B
Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome.
Campeau PM, Kim JC, Lu JT, Schwartzentruber JA, Abdul-Rahman OA, Schlaubitz S, Murdock DM, Jiang MM, Lammer EJ, Enns GM, Rhead WJ, Rowland J, Robertson SP, Cormier-Daire V, Bainbridge MN, Yang XJ, Gingras MC, Gibbs RA, Rosenblatt DS, Majewski J, Lee BH.
Am J Hum Genet 90(2):282-9. Epub 2012 Jan 19. 2012
7GPATS, KAT6B
De Novo Mutations of the Gene Encoding the Histone Acetyltransferase KAT6B Cause Genitopatellar Syndrome.
Simpson MA, Deshpande C, Dafou D, Vissers LE, Woollard WJ, Holder SE, Gillessen-Kaesbach G, Derks R, White SM, Cohen-Snuijf R, Kant SG, Hoefsloot LH, Reardon W, Brunner HG, Bongers EM, Trembath RC.
Am J Hum Genet 90(2):290-4. Epub 2012 Jan 19. 2012
8KAT6A, KAT6B
Tandem PHD fingers of MORF/MOZ acetyltransferases display selectivity for acetylated histone H3 and are required for the association with chromatin.
Ali M, Yan K, Lalonde ME, Degerny C, Rothbart SB, Strahl BD, Côté J, Yang XJ, Kutateladze TG.
J Mol Biol 424(5):328-38. doi: 10.1016/j.jmb.2012.10.004. Epub 2012 Oct 12. 2012
9KAT6B
Querkopf is a key marker of self-renewal and multipotency of adult neural stem cells.
Sheikh BN, Dixon MP, Thomas T, Voss AK.
J Cell Sci 125(Pt 2):295-309. doi: 10.1242/jcs.077271. Epub 2012 Feb 13. 2012
10GPATS, KAT6B, OHDO
The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms.
Campeau PM, Lu JT, Dawson BC, Fokkema IF, Robertson SP, Gibbs RA, Lee BH.
Hum Mutat 33(11):1520-5. doi: 10.1002/humu.22141. Epub 2012 Jul 12. Review. 2012
11BRD1, BRPF1, BRPF3, KAT6A, KAT6B
Recognition of unmodified histone H3 by the first PHD finger of bromodomain-PHD finger protein 2 provides insights into the regulation of histone acetyltransferases monocytic leukemic zinc-finger protein (MOZ) and MOZ-related factor (MORF).
Qin S, Jin L, Zhang J, Liu L, Ji P, Wu M, Wu J, Shi Y.
J Biol Chem 286(42):36944-55. doi: 10.1074/jbc.M111.244400. Epub 2011 Aug 31. 2011
12KAT6B, OHDO
Whole-Exome-Sequencing Identifies Mutations in Histone Acetyltransferase Gene KAT6B in Individuals with the Say-Barber-Biesecker Variant of Ohdo Syndrome.
Clayton-Smith J, O'Sullivan J, Daly S, Bhaskar S, Day R, Anderson B, Voss AK, Thomas T, Biesecker LG, Smith P, Fryer A, Chandler KE, Kerr B, Tassabehji M, Lynch SA, Krajewska-Walasek M, McKee S, Smith J, Sweeney E, Mansour S, Mohammed S, Donnai D, Black G.
Am J Hum Genet 89(5):675-81. 2011
13BRD1, BRPF1, BRPF3, ING5, KAT6A, KAT6B, MEAF6
Molecular architecture of quartet MOZ/MORF histone acetyltransferase complexes.
Ullah M, Pelletier N, Xiao L, Zhao SP, Wang K, Degerny C, Tahmasebi S, Cayrou C, Doyon Y, Goh SL, Champagne N, Côté J, Yang XJ.
Mol Cell Biol 28(22):6828-43. Epub 2008 Sep 15. Erratum in: Mol Cell Biol. 2009 Feb;29(3):942. PMID: 18794358 2008
14KAT6B
Investigation of MYST4 histone acetyltransferase and its involvement in mammalian gametogenesis.
McGraw S, Morin G, Vigneault C, Leclerc P, Sirard MA.
BMC Dev Biol 7:123.PMID: 17980037 2007
15KAT6A, KAT6B
MOZ and MORF, two large MYSTic HATs in normal and cancer stem cells.
Yang XJ, Ullah M.
Oncogene 26(37):5408-19. Review.PMID: 17694082 2007
16KAT6A, KAT6B
Functions of myst family histone acetyltransferases and their link to disease.
Avvakumov N, Côté J.
Subcell Biochem 41:295-317. Review.PMID: 17484133 2007
17KAT6B
The transcriptional coactivator Querkopf controls adult neurogenesis.
Merson TD, Dixon MP, Collin C, Rietze RL, Bartlett PF, Thomas T, Voss AK.
J Neurosci 26(44):11359-70.PMID: 17079664 2006
18KAT6B
Uterine leiomyomata with t(10;17) disrupt the histone acetyltransferase MORF.
Moore SD, Herrick SR, Ince TA, Kleinman MS, Dal Cin P, Morton CC, Quade BJ.
Cancer Res 64(16):5570-7.PMID: 15313893 2004
19CREBBP, KAT6B
t(10;16)(q22;p13) and MORF-CREBBP fusion is a recurrent event in acute myeloid leukemia.
Vizmanos JL, Larrayoz MJ, Lahortiga I, Floristan F, Alvarez C, Odero MD, Novo FJ, Calasanz MJ.
Genes Chromosomes Cancer 36(4):402-5. 2003
20ACTG1, COL1A1, COL1A2, COL2A1, COL9A1, DIO2, HSPA8, IBSP, IGF1, KAT6B, OGN, POU3F4, RBMS3, VIM, ZIC2
Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAs.
Luijendijk MW, van de Pol TJ, van Duijnhoven G, den Hollander AI, ten Caat J, van Limpt V, Brunner HG, Kremer H, Cremers FP.
Genomics 82(4):480-90. 2003
21AMLT3, KAT6A, KAT6B
MOZ and MORF histone acetyltransferases interact with the Runt-domain transcription factor Runx2.
Pelletier N, Champagne N, Stifani S, Yang XJ.
Oncogene 21(17):2729-40. 2002
22CREBBP, KAT6B
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13).
Panagopoulos I, Fioretos T, Isaksson M, Samuelsson U, Billstrom R, Strombeck B, Mitelman F, Johansson B.
Hum Mol Genet 10(4):395-404. 2001
23KAT6B
Identification of a human histone acetyltransferase related to monocytic leukemia zinc finger protein.
Champagne N, Bertos NR, Pelletier N, Wang AH, Vezmar M, Yang Y, Heng HH, Yang XJ.
J Biol Chem 274(40):28528-36. 1999
24ADAMTS3, AKAP6, ALMS1, ANKRD28, AREL1, ARHGEF10, ARHGEF11, ARHGEF17, ARNT2, BAZ2A, CABIN1, CAST, CHD9, CIC, CLEC16A, CLOCK, CTNND1, DCLK1, DDX46, DIDO1, DNAH9, DNM3, DOCK3, DYNC1H1, ECM29, ENTPD4, EPB41L1, EZH1, FRMPD4, GCC2, HECW1, HERC2, HISPPD1, HUWE1, IGSF1, KAT6B, KHNYN, KIAA0319, KIAA0355, KIAA0379, KIF3B, KMT2B, LBA1, MADD, MAST4, MCF2L, MDN1, MTMR3, MYO6, N4BP3, NACAD, NRCAM, PCDH9, PCDHGA8, PCDHGC3, PDZD2, PER2, PFAS, PLEKHM1, PLXNB2, PRORP, PRUNE2, PTPRN2, RAPGEF2, RIMBP2, RIMS1, RIPOR2, RUSC2, SALL2, SEC16A, SEMA3C, SEMA3E, SETD1A, SFRS14, SNPH, SPECC1L, SPTBN2, SR140, SRCAP, SRRM2, SYNJ2, TECPR2, TLN2, TRIM66, TTC37, UBR2, WNK1, XPO6, ZBTB39, ZBTB5, ZFYVE16, ZFYVE26, ZMYM3, ZNF518A, ZNF609, ZNF629, ZNF646
Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.
Nagase T, Ishikawa K, Nakajima D, Ohira M, Seki N, Miyajima N, Tanaka A,Kotani H, Nomura N, Ohara O.
DNA Res 4(2):141-50. 1997