TLX3
From Wikipedia, the free encyclopedia
T-cell leukemia homeobox 3
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Identifiers | ||||||||||||||
Symbol(s) | TLX3; HOX11L2; MGC29804; RNX | |||||||||||||
External IDs | OMIM: 604640 MGI: 1351209 HomoloGene: 23181 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 30012 | 27140 | ||||||||||||
Ensembl | ENSG00000164438 | ENSMUSG00000040610 | ||||||||||||
Uniprot | O43711 | Q5SQB4 | ||||||||||||
Refseq | NM_021025 (mRNA) NP_066305 (protein) |
NM_019916 (mRNA) NP_064300 (protein) |
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Location | Chr 5: 170.67 - 170.67 Mb | Chr 11: 33.1 - 33.1 Mb | ||||||||||||
Pubmed search | [1] | [2] |
T-cell leukemia homeobox 3, also known as TLX3, is a human gene.[1]
RNX (HOX11L2, TLX3) belongs to a family of orphan homeobox genes that encode DNA-binding nuclear transcription factors. Members of the HOX11 gene family are characterized by a threonine-47 replacing cytosine in the highly conserved homeodomain (Dear et al., 1993).[supplied by OMIM][1]
[edit] References
[edit] Further reading
- Dear TN, Sanchez-Garcia I, Rabbitts TH (1993). "The HOX11 gene encodes a DNA-binding nuclear transcription factor belonging to a distinct family of homeobox genes.". Proc. Natl. Acad. Sci. U.S.A. 90 (10): 4431-5. PMID 8099440.
- Cinti R, Fava M, Sancandi M, et al. (2001). "Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization.". Cytogenet. Cell Genet. 92 (3-4): 354-5. PMID 11435716.
- Lee-Kirsch MA, Engel K, Paditz E, et al. (2001). "Assignment of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34-->q35 by radiation hybrid mapping.". Cytogenet. Cell Genet. 92 (3-4): 358. PMID 11435718.
- Bernard OA, Busson-LeConiat M, Ballerini P, et al. (2002). "A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia.". Leukemia 15 (10): 1495-504. PMID 11587205.
- Ballerini P, Blaise A, Busson-Le Coniat M, et al. (2002). "HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis.". Blood 100 (3): 991-7. doi: . PMID 12130513.
- Matera I, Bachetti T, Cinti R, et al. (2003). "Mutational analysis of the RNX gene in congenital central hypoventilation syndrome.". Am. J. Med. Genet. 113 (2): 178-82. doi: . PMID 12407709.
- Mauvieux L, Leymarie V, Helias C, et al. (2003). "High incidence of Hox11L2 expression in children with T-ALL.". Leukemia 16 (12): 2417-22. doi: . PMID 12454747.
- 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: . PMID 12477932.
- Berger R, Dastugue N, Busson M, et al. (2003). "t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH).". Leukemia 17 (9): 1851-7. doi: . PMID 12970786.
- Cavé H, Suciu S, Preudhomme C, et al. (2004). "Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951.". Blood 103 (2): 442-50. doi: . PMID 14504110.
- Su XY, Busson M, Della Valle V, et al. (2004). "Various types of rearrangements target TLX3 locus in T-cell acute lymphoblastic leukemia.". Genes Chromosomes Cancer 41 (3): 243-9. doi: . PMID 15334547.
- 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: . PMID 15489334.
- Ballerini P, Busson M, Fasola S, et al. (2005). "NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance.". Leukemia 19 (3): 468-70. doi: . PMID 15674415.
- Gottardo NG, Jacoby PA, Sather HN, et al. (2005). "Significance of HOX11L2/TLX3 expression in children with T-cell acute lymphoblastic leukemia treated on Children's Cancer Group protocols.". Leukemia 19 (9): 1705-8. doi: . PMID 15990867.
- Borghini S, Vargiolu M, Di Duca M, et al. (2006). "Nuclear factor Y drives basal transcription of the human TLX3, a gene overexpressed in T-cell acute lymphocytic leukemia.". Mol. Cancer Res. 4 (9): 635-43. doi: . PMID 16966433.
- Nagel S, Scherr M, Kel A, et al. (2007). "Activation of TLX3 and NKX2-5 in t(5;14)(q35;q32) T-cell acute lymphoblastic leukemia by remote 3'-BCL11B enhancers and coregulation by PU.1 and HMGA1.". Cancer Res. 67 (4): 1461-71. doi: . PMID 17308084.