Citations for
1SATB2, UPF3B
Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene.
Leoyklang P, Suphapeetiporn K, Srichomthong C, Tongkobpetch S, Fietze S, Dorward H, Cullinane AR, Gahl WA, Huizing M, Shotelersuk V.
Hum Genet 132(12):1383-93. doi: 10.1007/s00439-013-1345-9. Epub 2013 Aug 8. 2013
2SATB2, SKI
Protooncogene Ski cooperates with the chromatin-remodeling factor Satb2 in specifying callosal neurons.
Baranek C, Dittrich M, Parthasarathy S, Bonnon CG, Britanova O, Lanshakov D, Boukhtouche F, Sommer JE, Colmenares C, Tarabykin V, Atanasoski S.
Proc Natl Acad Sci U S A. 109(9):3546-51 2012
3SATB1, SATB2
Satb1 and Satb2 are dispensable for X chromosome inactivation in mice.
Nechanitzky R, Dávila A, Savarese F, Fietze S, Grosschedl R.
Dev Cell 23(4):866-71. doi: 10.1016/j.devcel.2012.09.018. 2012
4SATB1, SATB2
SATB homeobox proteins regulate trophoblast stem cell renewal and differentiation.
Asanoma K, Kubota K, Chakraborty D, Renaud SJ, Wake N, Fukushima K, Soares MJ, Rumi MA.
J Biol Chem 287(3):2257-68. doi: 10.1074/jbc.M111.287128. Epub 2011 Nov 28. 2012
5DEL2Q32, SATB2
Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.
Balasubramanian M, Smith K, Basel-Vanagaite L, Feingold MF, Brock P, Gowans GC, Vasudevan PC, Cresswell L, Taylor EJ, Harris CJ, Friedman N, Moran R, Feret H, Zackai EH, Theisen A, Rosenfeld JA, Parker MJ.
J Med Genet 48(5):290-8. Epub 2011 Feb 22. 2011
6SATB2, SP7
Osteoblast-specific transcription factor Osterix (Osx) is an upstream regulator of Satb2 during bone formation.
Tang W, Li Y, Osimiri L, Zhang C.
J Biol Chem 286(38):32995-3002. Epub 2011 Aug 2. 2011
7SATB2, TP63
Special AT-rich binding protein-2 (SATB2) differentially affects disease-causing p63 mutant proteins.
Chung J, Grant RI, Kaplan DR, Irwin MS.
J Biol Chem 286(47):40671-80. doi: 10.1074/jbc.M111.271189. Epub 2011 Sep 29. 2011
8NANOG, SATB1, SATB2
Satb1 and Satb2 regulate embryonic stem cell differentiation and Nanog expression.
Savarese F, Dávila A, Nechanitzky R, De La Rosa-Velazquez I, Pereira CF, Engelke R, Takahashi K, Jenuwein T, Kohwi-Shigematsu T, Fisher AG, Grosschedl R.
Genes Dev 23(22):2625-38.PMID: 19933152 2009
9DEL2Q32, SATB2
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.
Rosenfeld JA, Ballif BC, Lucas A, Spence EJ, Powell C, Aylsworth AS, Torchia BA, Shaffer LG.
PLoS One 4(8):e6568.PMID: 19668335 2009
10SATB1, SATB2
The mRNA expression of SATB1 and SATB2 in human breast cancer.
Patani N, Jiang W, Mansel R, Newbold R, Mokbel K.
Cancer Cell Int 9:18.PMID: 19642980 2009
11SATB2
Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2.
Tegay DH, Chan KK, Leung L, Wang C, Burkett S, Stone G, Stanyon R, Toriello HV, Hatchwell E.
Clin Genet 75(3):259-64.PMID: 19170718 2009
12DEL2Q32, SATB2
4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate.
Urquhart J, Black GC, Clayton-Smith J.
Eur J Med Genet 52(6):454-7. Epub 2009 Jul 1.PMID: 19576302 2009
13SATB2
SATB2 interacts with chromatin-remodeling molecules in differentiating cortical neurons.
Gyorgy AB, Szemes M, de Juan Romero C, Tarabykin V, Agoston DV.
Eur J Neurosci 27(4):865-73.PMID: 18333962 2008
14SATB2
SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation.
Dobreva G, Chahrour M, Dautzenberg M, Chirivella L, Kanzler B, Farinas I, Karsenty G, Grosschedl R.
Cell 125(5):971-86. 2006
15DEL2Q32, SATB2
Satb2 Haploinsufficiency Phenocopies 2q32-q33 Deletions, whereas Loss Suggests a Fundamental Role in the Coordination of Jaw Development.
Britanova O, Depew MJ, Schwark M, Thomas BL, Miletich I, Sharpe P, Tarabykin V.
Am J Hum Genet 79(4):668-78. Epub 2006 Aug 30. 2006
16TGFA, SATB2, OFC2, OFC7
Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.
Beaty TH, Hetmanski JB, Fallin MD, Park JW, Sull JW, McIntosh I, Liang KY, Vanderkolk CA, Redett RJ, Boyadjiev SA, Jabs EW, Chong SS, Cheah FS, Wu-Chou YH, Chen PK, Chiu YF, Yeow V, Ng IS, Cheng J, Huang S, Ye X, Wang H, Ingersoll R, Scott AF.
Hum Genet 120(4):501-18. Epub 2006 Sep 5. 2006
17SATB1, SATB2
Novel transcription factor Satb2 interacts with matrix attachment region DNA elements in a tissue-specific manner and demonstrates cell-type-dependent expression in the developing mouse CNS.
Britanova O, Akopov S, Lukyanov S, Gruss P, Tarabykin V.
Eur J Neurosci 21(3):658-68.PMID: 15733084 2005
18FOXE1, HTAT, IRF6, MSX1, NECTIN1, OFC2, OFC5, OFC6, OFC6, SATB2, SCD5, TP63
Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.
Stanier P, Moore GE.
Hum Mol Genet 13 Spec No 1:R73-81. Epub 2004 Jan 13. 2004
19DEL2Q32, OFC7, SATB2
Identification of SATB2 as the cleft palate gene on 2q32-q33.
FitzPatrick DR, Carr IM, McLaren L, Leek JP, Wightman P, Williamson K, Gautier P, McGill N, Hayward C, Firth H, Markham AF, Fantes JA, Bonthron DT.
Hum Mol Genet 12(19):2491-501. Epub 2003 Jul 29. 2003
20SATB2
SUMO modification of a novel MAR-binding protein, SATB2, modulates immunoglobulin mu gene expression.
Dobreva G, Dambacher J, Grosschedl R.
Genes Dev. 17(24):3048-61. 2003
21DEL2Q32,SATB2, PRS, OFC7
Pierre Robin sequence and interstitial deletion 2q32.3-q33.2.
Houdayer C, Portnoi MF, Vialard F, Soupre V, Crumiere C, Taillemite JL, Couderc R, Vazquez MP, Bahuau M.
Am J Med Genet 102(3):219-26. 2001
22ABI2, AOX1, BMPR2, CASP10, CASP8, CD28, CFLAR, CLK1, CTLA4, DAZAP2, MAGI2, ORC2, PPH1, PSMA2, SATB2, SUMO1, TRAK2
A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension.
Machado RD, Pauciulo MW, Fretwell N, Veal C, Thomson JR, Vilarino Guell C, Aldred M, Brannon CA, Trembath RC, Nichols WC.
Genomics 68(2):220-8. 2000
23AAK1, ANKRD26, ARHGEF4, CEP131, CEP164, DOCK9, DOLK, DOPEY1, EPN2, GARNL4, HIC2, KIAA1033, KIAA1109, LIMCH1, LMTK2, MYT1, NLGN1, OTUD4, PDZRN3, PITRM1, PLCH1, PLCL2, PPM1E, RAP140, RBM16, RNF44, SAMD4A, SAPS1, SATB2, SLC8A2, SMG5, SON, SULF1, SV2C, SYNPO, TBC1D2B, TRAK1, TRIM33, TRIM35, TTC28, USP2, USP22, USP24, WDTC1, ZC3H4, ZFR2, ZNF507
Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Kikuno R, Nagase T, Ishikawa K, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O.
DNA Res 6(3):197-205. 1999