| 1 | ANKRD11, DEL16Q243, KBG
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| Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndrome.
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| Khalifa M, Stein J, Grau L, Nelson V, Meck J, Aradhya S, Duby J.
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| Am J Med Genet A 161(4):835-40. doi: 10.1002/ajmg.a.35739. Epub 2013 Mar 12.
2013
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| 2 | ANKRD11, KBG
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| Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations.
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| Lo-Castro A, Brancati F, Digilio MC, Garaci FG, Bollero P, Alfieri P, Curatolo P.
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| Am J Med Genet B Neuropsychiatr Genet 162B(1):17-23. doi: 10.1002/ajmg.b.32113. Epub 2012 Nov 26.
2013
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| 3 | ANKRD11, DEL16Q243, KBG
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| Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome.
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| Sacharow S, Li D, Fan YS, Tekin M.
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| Am J Med Genet A 158A(3):547-52. doi: 10.1002/ajmg.a.34436. Epub 2012 Feb 3.
2012
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| 4 | ANKRD11, DEL16Q243
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| Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms.
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| Isrie M, Hendriks Y, Gielissen N, Sistermans EA, Willemsen MH, Peeters H, Vermeesch JR, Kleefstra T, Van Esch H.
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| Eur J Hum Genet 20(2):131-3. doi: 10.1038/ejhg.2011.105. Epub 2011 Jun 8. No abstract available.
2012
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| 5 | ANKRD11, KBG
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| Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia.
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| Sirmaci A, Spiliopoulos M, Brancati F, Powell E, Duman D, Abrams A, Bademci G, Agolini E, Guo S, Konuk B, Kavaz A, Blanton S, Digilio MC, Dallapiccola B, Young J, Zuchner S, Tekin M.
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| Am J Hum Genet 89(2):289-94. Epub 2011 Jul 21.
2011
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| 6 | ANKRD11, DEL16Q243, ZNF778
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| Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
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| Willemsen MH, Fernandez BA, Bacino CA, Gerkes E, de Brouwer AP, Pfundt R, Sikkema-Raddatz B, Scherer SW, Marshall CR, Potocki L, van Bokhoven H, Kleefstra T.
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| Eur J Hum Genet 18(4):429-35. Epub 2009 Nov 18.PMID: 19920853 2010
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| 7 | ANKRD11, DEL15Q24, DEL16P112P, DELXP22, DPP10, DPP6, DPYD, NLGN4, NLGN4X, NRXN1, PCDH9, PTCHD1, SHANK3
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| Structural variation of chromosomes in autism spectrum disorder.
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| Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW.
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| Am J Hum Genet 82(2):477-88. Epub 2008 Jan 17. 2008
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| 8 | ANKRD11
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| Identification of ANKRD11 as a p53 coactivator.
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| Neilsen PM, Cheney KM, Li CW, Chen JD, Cawrse JE, Schulz RB, Powell JA, Kumar R, Callen DF.
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| J Cell Sci 121(Pt 21):3541-52. Epub 2008 Oct 7.
2008
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| 9 | ANKRD11, ANKRD12, TADA3
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| Ankyrin repeats-containing cofactors interact with ADA3 and modulate its co-activator function.
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| Li CW, Dinh GK, Zhang A, Chen JD.
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| Biochem J 413(2):349-57. 2008
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| 10 | ANKRD11
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| Subcellular localization of ankyrin repeats cofactor-1 regulates its corepressor activity.
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| Zhang A, Li CW, Tsai SC, Chen JD.
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| J Cell Biochem 101(5):1301-15.
2007
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| 11 | ANKRD11
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| Identification of a novel family of ankyrin repeats containing cofactors for p160 nuclear receptor coactivators.
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| Zhang A, Yeung PL, Li CW, Tsai SC, Dinh GK, Wu X, Li H, Chen JD.
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| J Biol Chem 279(32):33799-805. Epub 2004 Jun 7.
2004
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| 12 | ANKRD11, ANKRD11, ATAD2, C14orf57, FOXN3, GSDMB, HEMGN, KCTD9, LMAN1L, NUSAP1, PBRM1, PHACTR4, PPP4R1L, PRO1880, PRO2133, SSU72, SYAP1, USP39, ZC3HAV1, ZFP91
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| Gene expression profiling in human fetal liver and identification of tissue- and developmental-stage-specific genes through compiled expression profiles and efficient cloning of full-length cDNAs.
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| Yu Y, Zhang C, Zhou G, Wu S, Qu X, Wei H, Xing G, Dong C, Zhai Y, Wan J,Ouyang S, Li L, Zhang S, Zhou K, Zhang Y, Wu C, He F.
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| Genome Res 11(8):1392-403. 2001
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