| 1 | MNX1, SCRA
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| Phenotype analysis impacts testing strategy in patients with Currarino syndrome.
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| Cuturilo G, Hodge JC, Runke CK, Thorland EC, Al-Owain MA, Ellison JW, Babovic-Vuksanovic D.
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| Clin Genet lin Genet. 2015 Feb 18. doi: 10.1111/cge.12572. [Epub ahead of print]
2015
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| 2 | MNX1, NKX2-2
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| Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in man.
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| Flanagan SE, De Franco E, Lango Allen H, Zerah M, Abdul-Rasoul MM, Edge JA, Stewart H, Alamiri E, Hussain K, Wallis S, de Vries L, Rubio-Cabezas O, Houghton JA, Edghill EL, Patch AM, Ellard S, Hattersley AT.
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| Cell Metab 19(1):146-54. doi: 10.1016/j.cmet.2013.11.021.
2014
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| 3 | CRA, DELQ36, MNX1
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| Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH Gene.
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| Coutton C, Poreau B, Devillard F, Durand C, Odent S, Rozel C, Vieville G, Amblard F, Jouk PS, Satre V.
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| Mol Syndromol 5(1):25-31. doi: 10.1159/000355391. Epub 2013 Oct 2.
2014
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| 4 | MNX1, SCRA
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| Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.
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| Merello E, De Marco P, Ravegnani M, Riccipetitoni G, Cama A, Capra V.
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| Eur J Med Genet 56(12):648-54. doi: 10.1016/j.ejmg.2013.09.011. Epub 2013 Oct 3.
2013
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| 5 | MNX1, PRDM5
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| Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family.
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| Bonnefond A, Vaillant E, Philippe J, Skrobek B, Lobbens S, Yengo L, Huyvaert M, Cavé H, Busiah K, Scharfmann R, Polak M, Abdul-Rasoul M, Froguel P, Vaxillaire M.
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| Diabetes Metab 39(3):276-80. doi: 10.1016/j.diabet.2013.02.007. Epub 2013 Apr 4.
2013
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| 6 | MNX1
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| The embryonic transcription factor Hlxb9 is a menin interacting partner that controls pancreatic β-cell proliferation and the expression of insulin regulators.
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| Shi K, Parekh VI, Roy S, Desai SS, Agarwal SK.
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| Endocr Relat Cancer 20(1):111-22. doi: 10.1530/ERC-12-0077. Print 2013 Feb.
2013
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| 7 | MNX1
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| Mnx1: a gatekeeper of β cell fate.
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| Dalgin G, Prince VE.
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| Islets 4(4):320-2. doi: 10.4161/isl.21984. Epub 2012 Jul 1.
2012
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| 8 | MNX1
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| The dual role of HLXB9 in leukemia.
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| Ferguson S, Gautrey HE, Strathdee G.
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| Pediatr Blood Cancer 56(3):349-52. doi: 10.1002/pbc.22679.
2011
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| 9 | MNX1, SCRA
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| MNX1 (HLXB9) mutations in Currarino patients.
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| Garcia-Barceló MM, Lui VC, So MT, Miao X, Leon TY, Yuan ZW, Ngan ES, Ehsan T, Chung PH, Khong PL, Wong KK, Tam PK.
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| J Pediatr Surg 44(10):1892-8. doi: 10.1016/j.jpedsurg.2009.03.039.
2009
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| 10 | SCRA, MNX1, DEL7Q36
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| Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
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| CrŽtolle C, Pelet A, Sanlaville D, ZŽrah M, Amiel J, Jaubert F, RŽvillon Y, Baala L, Munnich A, Nihoul-FŽkŽtŽ C, Lyonnet S.
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| Hum Mutat 29(7):903-10. 2008
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| 11 | MNX1, SCRA
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| Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
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| Crétolle C, Pelet A, Sanlaville D, Zérah M, Amiel J, Jaubert F, Révillon Y, Baala L, Munnich A, Nihoul-Fékété C, Lyonnet S.
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| Hum Mutat 29(7):903-10.
2008
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| 12 | MNX1
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| Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome.
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| Kim IS, Oh SY, Choi SJ, Kim JH, Park KH, Park HK, Kim JW, Ki CS.
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| J Hum Genet 52(8):698-701. Epub 2007 Jul 6. 2007
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| 13 | MNX1, ETV6
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| High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.
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| von Bergh AR, van Drunen E, van Wering ER, van Zutven LJ, Hainmann I, Lonnerholm G, Meijerink JP, Pieters R, Beverloo HB.
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| Genes Chromosomes Cancer 45(8):731-9. 2006
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| 14 | ALX4, PFM1, MNX1, SCRA, VSX1, KTCN1, VSX2, MCIA, SOPT, HESX1, HOXD13, PSDY2, MSX2, PFM2, SIX3, HPE2, DCS, SHOX
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| Homeodomain revisited: a lesson from disease-causing mutations.
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| Chi YI.
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| Hum Genet 116(6):433-44. Epub 2005 Feb 23. 2005
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| 15 | HPE3, SCRA, MNX1, SHH, DEL7Q36
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| Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3.
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| Horn D, Tonnies H, Neitzel H, Wahl D, Hinkel GK, von Moers A, Bartsch O.
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| Am J Med Genet A 128(1):85-92. 2004
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| 16 | MNX1, DEL7Q36
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| Terminal deletion of the chromosome 7(q36-qter) in an infant with sacral agenesis and anterior myelomeningocele.
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| Rodriguez L, Cuadrado Perez I, Herrera Montes J, Lorente Jareno ML, Lopez Grondona F, Martinez-Frias ML.
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| Am J Med Genet 110(1):73-7. 2002
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| 17 | MNX1, SCRA, DEL7Q36
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| Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome.
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| Kochling J, Karbasiyan M, Reis A.
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| Eur J Hum Genet 9(8):599-605. 2001
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| 18 | MNX1
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| Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13).
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| Beverloo HB, Panagopoulos I, Isaksson M, van Wering E, van Drunen E, de Klein A, Johansson B, Slater R.
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| Cancer Res 61(14):5374-7. 2001
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| 19 | MNX1, DEL7Q36
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| Involvement of the HLXB9 homeobox gene in Currarino syndrome.
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| Belloni E, Martucciello G, Verderio D, Ponti E, Seri M, Jasonni V, Torre M, Ferrari M, Tsui LC, Scherer SW.
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| Am J Hum Genet 66(1):312-9. No abstract available. 2000
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| 20 | MNX1, SCRA, DEL7Q36
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| Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.
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| Hagan DM, Ross AJ, Strachan T, Lynch SA, Ruiz-Perez V, Wang YM, Scambler P, Custard E, Reardon W, Hassan S, Muenke M, Nixon P, Papapetrou C, Winter RM, Edwards Y, Morrison K, Barrow M, Cordier-Alex MP, Correia P, Galvin-Parton PA, Gaskill S, Gaskin KJ, Garcia-Minaur S, Gereige R, Hayward R, Homfray T.
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| Am J Hum Genet 66(5):1504-15. 2000
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| 21 | MNX1, SCRA
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| A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.
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| Ross AJ, et al.
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| Nat Genet 20 : 358-361. 1998
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| 22 | MNX1
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| A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues.
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| Harrison KA, et al.
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| J Biol Chem 269 : 19968-19975. 1994
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| 23 | HLX, MNX1
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| Two diverged human homeobox genes involved in the differentiation of human hematopoietic progenitors map to chromosome 1, bands q41-42.1.
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| Najfeld V, et al.
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| Genes Chromosomes Cancer 5 : 343-347. 1992
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