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MEOX2 - Wikipedia, the free encyclopedia

MEOX2

From Wikipedia, the free encyclopedia


Mesenchyme homeobox 2
Identifiers
Symbol(s) MEOX2; GAX; MOX2
External IDs OMIM: 600535 MGI103219 HomoloGene4330
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 4223 17286
Ensembl ENSG00000106511 ENSMUSG00000036144
Uniprot P50222 Q99M23
Refseq NM_005924 (mRNA)
NP_005915 (protein)
NM_008584 (mRNA)
NP_032610 (protein)
Location Chr 7: 15.62 - 15.69 Mb Chr 12: 37.62 - 37.69 Mb
Pubmed search [1] [2]

Mesenchyme homeobox 2, also known as MEOX2, is a human gene.[1]

This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.[1]

[edit] References

[edit] Further reading

  • Grigoriou M, Kastrinaki MC, Modi WS, et al. (1995). "Isolation of the human MOX2 homeobox gene and localization to chromosome 7p22.1-p21.3.". Genomics 26 (3): 550-5. PMID 7607679. 
  • LePage DF, Altomare DA, Testa JR, Walsh K (1995). "Molecular cloning and localization of the human GAX gene to 7p21.". Genomics 24 (3): 535-40. doi:10.1006/geno.1994.1663. PMID 7713505. 
  • Reardon W, McManus SP, Summers D, Winter RM (1994). "Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2.". Am. J. Med. Genet. 47 (5): 633-6. doi:10.1002/ajmg.1320470510. PMID 8266988. 
  • Quinn LM, Latham SE, Kalionis B (2000). "The homeobox genes MSX2 and MOX2 are candidates for regulating epithelial-mesenchymal cell interactions in the human placenta.". Placenta 21 Suppl A: S50-4. PMID 10831122. 
  • Stamataki D, Kastrinaki M, Mankoo BS, et al. (2001). "Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors.". FEBS Lett. 499 (3): 274-8. PMID 11423130. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Scherer SW, Cheung J, MacDonald JR, et al. (2003). "Human chromosome 7: DNA sequence and biology.". Science 300 (5620): 767-72. doi:10.1126/science.1083423. PMID 12690205. 
  • Gorski DH, Leal AJ (2003). "Inhibition of endothelial cell activation by the homeobox gene Gax.". J. Surg. Res. 111 (1): 91-9. PMID 12842453. 
  • Hillier LW, Fulton RS, Fulton LA, et al. (2003). "The DNA sequence of human chromosome 7.". Nature 424 (6945): 157-64. doi:10.1038/nature01782. PMID 12853948. 
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334. 
  • Wu Z, Guo H, Chow N, et al. (2005). "Role of the MEOX2 homeobox gene in neurovascular dysfunction in Alzheimer disease.". Nat. Med. 11 (9): 959-65. doi:10.1038/nm1287. PMID 16116430. 
  • Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173-8. doi:10.1038/nature04209. PMID 16189514. 
  • Lin J, Friesen MT, Bocangel P, et al. (2006). "Characterization of Mesenchyme Homeobox 2 (MEOX2) transcription factor binding to RING finger protein 10.". Mol. Cell. Biochem. 275 (1-2): 75-84. PMID 16335786. 
  • Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.". Genome Res. 16 (1): 55-65. doi:10.1101/gr.4039406. PMID 16344560. 
  • Chen Y, Leal AD, Patel S, Gorski DH (2007). "The homeobox gene GAX activates p21WAF1/CIP1 expression in vascular endothelial cells through direct interaction with upstream AT-rich sequences.". J. Biol. Chem. 282 (1): 507-17. doi:10.1074/jbc.M606604200. PMID 17074759. 

[edit] External links


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


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