Mutations in the MNX1 gene are associated with Currarino syndrome.[6] Upregulated expression of MNX1-AS1 long noncoding RNA predicts poor prognosis in gastric cancer.[7]
^Merello E, De Marco P, Ravegnani M, Riccipetitoni G, Cama A, Capra V (2013). "Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases". Eur J Med Genet. 56 (12): 648–54. doi:10.1016/j.ejmg.2013.09.011. PMID24095820.648-54&rft.date=2013&rft_id=info:doi/10.1016/j.ejmg.2013.09.011&rft_id=info:pmid/24095820&rft.aulast=Merello&rft.aufirst=E&rft.au=De Marco, P&rft.au=Ravegnani, M&rft.au=Riccipetitoni, G&rft.au=Cama, A&rft.au=Capra, V&rfr_id=info:sid/en.wikipedia.org:MNX1" class="Z3988">
^ Zhang, W., Huang, L., Lu, X., Wang, K., Ning, X., & Liu, Z. (2019). Upregulated expression of MNX1-AS1 long noncoding RNA predicts poor prognosis in gastric cancer. Bosnian journal of basic medical sciences, 19(2), 164–171. https://doi.org/10.17305/bjbms.2019.3713
Ross AJ, Ruiz-Perez V, Wang Y, Hagan DM, Scherer S, Lynch SA, Lindsay S, Custard E, Belloni E, Wilson DI, Wadey R, Goodman F, Orstavik KH, Monclair T, Robson S, Reardon W, Burn J, Scambler P, Strachan T (1998). "A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis". Nat. Genet. 20 (4): 358–61. doi:10.1038/3828. PMID9843207. S2CID31062371.358-61&rft.date=1998&rft_id=https://api.semanticscholar.org/CorpusID:31062371#id-name=S2CID&rft_id=info:pmid/9843207&rft_id=info:doi/10.1038/3828&rft.aulast=Ross&rft.aufirst=AJ&rft.au=Ruiz-Perez, V&rft.au=Wang, Y&rft.au=Hagan, DM&rft.au=Scherer, S&rft.au=Lynch, SA&rft.au=Lindsay, S&rft.au=Custard, E&rft.au=Belloni, E&rft.au=Wilson, DI&rft.au=Wadey, R&rft.au=Goodman, F&rft.au=Orstavik, KH&rft.au=Monclair, T&rft.au=Robson, S&rft.au=Reardon, W&rft.au=Burn, J&rft.au=Scambler, P&rft.au=Strachan, T&rfr_id=info:sid/en.wikipedia.org:MNX1" class="Z3988">
Heus HC, Hing A, van Baren MJ, Joosse M, Breedveld GJ, Wang JC, Burgess A, Donnis-Keller H, Berglund C, Zguricas J, Scherer SW, Rommens JM, Oostra BA, Heutink P (1999). "A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36". Genomics. 57 (3): 342–51. doi:10.1006/geno.1999.5796. PMID10329500.342-51&rft.date=1999&rft_id=info:doi/10.1006/geno.1999.5796&rft_id=info:pmid/10329500&rft.aulast=Heus&rft.aufirst=HC&rft.au=Hing, A&rft.au=van Baren, MJ&rft.au=Joosse, M&rft.au=Breedveld, GJ&rft.au=Wang, JC&rft.au=Burgess, A&rft.au=Donnis-Keller, H&rft.au=Berglund, C&rft.au=Zguricas, J&rft.au=Scherer, SW&rft.au=Rommens, JM&rft.au=Oostra, BA&rft.au=Heutink, P&rfr_id=info:sid/en.wikipedia.org:MNX1" class="Z3988">
Belloni E, Martucciello G, Verderio D, Ponti E, Seri M, Jasonni V, Torre M, Ferrari M, Tsui LC, Scherer SW (2000). "Involvement of the HLXB9 homeobox gene in Currarino syndrome". Am. J. Hum. Genet. 66 (1): 312–9. doi:10.1086/302723. PMC1288336. PMID10631160.312-9&rft.date=2000&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288336#id-name=PMC&rft_id=info:pmid/10631160&rft_id=info:doi/10.1086/302723&rft.aulast=Belloni&rft.aufirst=E&rft.au=Martucciello, G&rft.au=Verderio, D&rft.au=Ponti, E&rft.au=Seri, M&rft.au=Jasonni, V&rft.au=Torre, M&rft.au=Ferrari, M&rft.au=Tsui, LC&rft.au=Scherer, SW&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288336&rfr_id=info:sid/en.wikipedia.org:MNX1" class="Z3988">
Hagan DM, Ross AJ, Strachan T, Lynch SA, Ruiz-Perez V, Wang YM, Scambler P, Custard E, Reardon W, Hassan S, 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 (2000). "Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene". Am. J. Hum. Genet. 66 (5): 1504–15. doi:10.1086/302899. PMC1378009. PMID10749657.1504-15&rft.date=2000&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1378009#id-name=PMC&rft_id=info:pmid/10749657&rft_id=info:doi/10.1086/302899&rft.aulast=Hagan&rft.aufirst=DM&rft.au=Ross, AJ&rft.au=Strachan, T&rft.au=Lynch, SA&rft.au=Ruiz-Perez, V&rft.au=Wang, YM&rft.au=Scambler, P&rft.au=Custard, E&rft.au=Reardon, W&rft.au=Hassan, S&rft.au=Nixon, P&rft.au=Papapetrou, C&rft.au=Winter, RM&rft.au=Edwards, Y&rft.au=Morrison, K&rft.au=Barrow, M&rft.au=Cordier-Alex, MP&rft.au=Correia, P&rft.au=Galvin-Parton, PA&rft.au=Gaskill, S&rft.au=Gaskin, KJ&rft.au=Garcia-Minaur, S&rft.au=Gereige, R&rft.au=Hayward, R&rft.au=Homfray, T&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1378009&rfr_id=info:sid/en.wikipedia.org:MNX1" class="Z3988">
Kapranov P, Drenkow J, Cheng J, Long J, Helt G, Dike S, Gingeras TR (2005). "Examples of the complex architecture of the human transcriptome revealed by RACE and high-density tiling arrays". Genome Res. 15 (7): 987–97. doi:10.1101/gr.3455305. PMC1172043. PMID15998911.987-97&rft.date=2005&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1172043#id-name=PMC&rft_id=info:pmid/15998911&rft_id=info:doi/10.1101/gr.3455305&rft.aulast=Kapranov&rft.aufirst=P&rft.au=Drenkow, J&rft.au=Cheng, J&rft.au=Long, J&rft.au=Helt, G&rft.au=Dike, S&rft.au=Gingeras, TR&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1172043&rfr_id=info:sid/en.wikipedia.org:MNX1" class="Z3988">
von Bergh AR, van Drunen E, van Wering ER, van Zutven LJ, Hainmann I, Lönnerholm G, Meijerink JP, Pieters R, Beverloo HB (2006). "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". Genes Chromosomes Cancer. 45 (8): 731–9. doi:10.1002/gcc.20335. PMID16646086. S2CID27381746.731-9&rft.date=2006&rft_id=https://api.semanticscholar.org/CorpusID:27381746#id-name=S2CID&rft_id=info:pmid/16646086&rft_id=info:doi/10.1002/gcc.20335&rft.aulast=von Bergh&rft.aufirst=AR&rft.au=van Drunen, E&rft.au=van Wering, ER&rft.au=van Zutven, LJ&rft.au=Hainmann, I&rft.au=Lönnerholm, G&rft.au=Meijerink, JP&rft.au=Pieters, R&rft.au=Beverloo, HB&rfr_id=info:sid/en.wikipedia.org:MNX1" class="Z3988">
Kim IS, Oh SY, Choi SJ, Kim JH, Park KH, Park HK, Kim JW, Ki CS (2007). "Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome". J. Hum. Genet. 52 (8): 698–701. doi:10.1007/s10038-007-0173-y. PMID17612791.698-701&rft.date=2007&rft_id=info:doi/10.1007/s10038-007-0173-y&rft_id=info:pmid/17612791&rft.aulast=Kim&rft.aufirst=IS&rft.au=Oh, SY&rft.au=Choi, SJ&rft.au=Kim, JH&rft.au=Park, KH&rft.au=Park, HK&rft.au=Kim, JW&rft.au=Ki, CS&rft_id=https://doi.org/10.1007%2Fs10038-007-0173-y&rfr_id=info:sid/en.wikipedia.org:MNX1" class="Z3988">