HOXA13 Gene

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Liu, D. HOXA13 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4103 (accessed on 28 September 2026).

Liu D. HOXA13 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4103. Accessed September 28, 2026.

Liu, Dean. "HOXA13 Gene" Encyclopedia, https://encyclopedia.pub/entry/4103 (accessed September 28, 2026).

Liu, D. (2020, December 23). HOXA13 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4103

Liu, Dean. "HOXA13 Gene." Encyclopedia. Web. 23 December, 2020.

HOXA13 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/hoxa13

Homeobox A13

genes

References

Fujino T, Suzuki A, Ito Y, Ohyashiki K, Hatano Y, Miura I, Nakamura T.Single-translocation and double-chimeric transcripts: detection of NUP98-HOXA9 inmyeloid leukemias with HOXA11 or HOXA13 breaks of the chromosomal translocationt(7;11)(p15;p15). Blood. 2002 Feb 15;99(4):1428-33.
Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, InnisJW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ.Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.Am J Hum Genet. 2000 Jul;67(1):197-202.
Goodman FR, Scambler PJ. Human HOX gene mutations. Clin Genet. 2001Jan;59(1):1-11. Review.
Goodman FR. Limb malformations and the human HOX genes. Am J Med Genet. 2002Oct 15;112(3):256-65. Review.
Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD,Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B. Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model. Hum Mol Genet. 2004 Nov 15;13(22):2841-51.
Innis JW. Hand-Foot-Genital Syndrome. 2006 Jul 11 [updated 2019 Aug 8]. In:Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A,editors. GeneReviews® [Internet]. Seattle (WA): University of Washington,Seattle; 1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK1423/
Mortlock DP, Innis JW. Mutation of HOXA13 in hand-foot-genital syndrome. NatGenet. 1997 Feb;15(2):179-80.
Taketani T, Taki T, Ono R, Kobayashi Y, Ida K, Hayashi Y. The chromosometranslocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of theNUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9. Genes ChromosomesCancer. 2002 Aug;34(4):437-43.
Utsch B, Becker K, Brock D, Lentze MJ, Bidlingmaier F, Ludwig M. A novelstable polyalanine [poly(A)] expansion in the HOXA13 gene associated withhand-foot-genital syndrome: proper function of poly(A)-harbouring transcriptionfactors depends on a critical repeat length? Hum Genet. 2002 May;110(5):488-94.
Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dötsch J, Ludwig M,Reutter H, Innis JW. Molecular characterization of HOXA13 polyalanine expansionproteins in hand-foot-genital syndrome. Am J Med Genet A. 2007 Dec15;143A(24):3161-8.

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Subjects: Genetics & Heredity

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