MNX1

Homeobox HB9
Identifiers
Symbols	MNX1 ;HLXB9; HB9; HOXHB9; SCRA1
External IDs	Template:OMIM5 Template:MGI HomoloGene: 21137
Gene ontology Molecular function Template:GNF GO Template:GNF GO Template:GNF GO Cellular component Template:GNF GO Biological process Template:GNF GO Template:GNF GO Template:GNF GO
RNA expression pattern
File:PBB GE HLXB9 214614 at tn.png
More reference expression data
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

Motor neuron and pancreas homeobox 1 (MNX1) also known as Homeobox HB9 (HLXB9), is a human gene.

Further reading

• Catala M (2002). "Genetic control of caudal development". Clin. Genet. 61 (2): 89–96. PMID 11940082.
• Deguchi Y, Kehrl JH (1991). "Nucleotide sequence of a novel diverged human homeobox gene encodes a DNA binding protein". Nucleic Acids Res. 19 (13): 3742. PMID 1677181.
• Deguchi Y, Kehrl JH (1991). "Selective expression of two homeobox genes in CD34-positive cells from human bone marrow". Blood. 78 (2): 323–8. PMID 1712647.
• Lynch SA, Bond PM, Copp AJ; et al. (1995). "A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36". Nat. Genet. 11 (1): 93–5. doi:10.1038/ng0995-93. PMID 7550324.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Harrison KA, Druey KM, Deguchi Y; et al. (1994). "A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues". J. Biol. Chem. 269 (31): 19968–75. PMID 7914194.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Ross AJ, Ruiz-Perez V, Wang Y; et al. (1998). "A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis". Nat. Genet. 20 (4): 358–61. doi:10.1038/3828. PMID 9843207.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Heus HC, Hing A, van Baren MJ; et al. (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. PMID 10329000.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Belloni E, Martucciello G, Verderio D; et al. (2000). "Involvement of the HLXB9 homeobox gene in Currarino syndrome". Am. J. Hum. Genet. 66 (1): 312–9. PMID 10631160.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Hagan DM, Ross AJ, Strachan T; et al. (2000). "Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene". Am. J. Hum. Genet. 66 (5): 1504–15. PMID 10749657.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Köchling J, Karbasiyan M, Reis A (2001). "Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome". Eur. J. Hum. Genet. 9 (8): 599–605. doi:10.1038/sj.ejhg.5200683. PMID 11528505.CS1 maint: Multiple names: authors list (link)
• Nagel S, Scherr M, Quentmeier H; et al. (2005). "HLXB9 activates IL6 in Hodgkin lymphoma cell lines and is regulated by PI3K signalling involving E2F3". Leukemia. 19 (5): 841–6. doi:10.1038/sj.leu.2403716. PMID 15772702.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Cheng J, Kapranov P, Drenkow J; et al. (2005). "Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution". Science. 308 (5725): 1149–54. doi:10.1126/science.1108625. PMID 15790807.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Hori Y, Gu X, Xie X, Kim SK (2006). "Differentiation of insulin-producing cells from human neural progenitor cells". PLoS Med. 2 (4): e103. doi:10.1371/journal.pmed.0020103. PMID 15839736.CS1 maint: Multiple names: authors list (link)
• Kapranov P, Drenkow J, Cheng J; et al. (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. PMID 15998911.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• von Bergh AR, van Drunen E, van Wering ER; et al. (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. PMID 16646086.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Kim IS, Oh SY, Choi SJ; et al. (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. PMID 17612791.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)

External links

• MNX1+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)

This article incorporates text from the United States National Library of Medicine, which is in the public domain.