Proc. Natl. Acad. Sci. U.S.A.

A common chromosomal abnormality in childhood T-cell acute leukemia is a translocation, t(10;14) (q24;q11), that together with the variant t(7;10)(q35;q24) is present in up to 7% of this tumor type. The gene adjacent to the 10q24 region is transcriptionally activated after translocation to either TCRD (14q11) or TCRB (7q35). It encodes a homeobox gene closely related to the developmentally regulated homeotic genes of flies and mammals. The coding capacity of this activated gene, designated HOX11, is undisturbed in a T-cell line carrying the translocation t(7;10)(q35;q24). Therefore, the HOX11 homeobox gene seems to be involved in T-cell tumorigenesis.

Source:http://purl.uniprot.org/citations/1681546

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
rdfs:comment
A common chromosomal abnormality in childhood T-cell acute leukemia is a translocation, t(10;14) (q24;q11), that together with the variant t(7;10)(q35;q24) is present in up to 7% of this tumor type. The gene adjacent to the 10q24 region is transcriptionally activated after translocation to either TCRD (14q11) or TCRB (7q35). It encodes a homeobox gene closely related to the developmentally regulated homeotic genes of flies and mammals. The coding capacity of this activated gene, designated HOX11, is undisturbed in a T-cell line carrying the translocation t(7;10)(q35;q24). Therefore, the HOX11 homeobox gene seems to be involved in T-cell tumorigenesis.
skos:exactMatch
uniprot:name
Proc. Natl. Acad. Sci. U.S.A.
uniprot:author
Boehm T., Dear T.N., Gonzalez-Sarmiento R., Kees U.R., Kennedy M.A., Lampert F., Rabbitts T.H.
uniprot:date
1991
uniprot:pages
8900-8904
uniprot:title
HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24.
uniprot:volume
88
dc-term:identifier
doi:10.1073/pnas.88.20.8900