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Allele : Tg(CTSG-RARA/PML)2683Ley transgene insertion 2683, Timothy Ley

Primary Identifier  MGI:3620139 Allele Type  Transgenic
Attribute String  Humanized sequence, Inserted expressed sequence Gene  Tg(CTSG-RARA/PML)2683Ley
Strain of Origin  Not Specified Is Recombinase  false
Is Wild Type  false
description  This is one of 4 germline-transmitting lines expressing this transgenic construct that are mentioned in J:59080, of which 2 are characterized in detail (but not distinguished from one another).

Leukemia in the doubly transgenic mice described above is a model for acute promyelocytic leukemia; see OMIM *102578: ACUTE PROMYELOCYTIC LEUKEMIA, INDUCER OF; PML

molecularNote  The functional cDNA coding sequence is derived from the breakpoint cluster region 3 (bcr-3) isoform transcript of the RARA/PML fusion gene resulting from the characteristic t(15;17)(q22;q11.2-q12) translocation associated with ~90% of human cases of acute promyelocytic leukemia (APML). The bcr-3 isoform of the chimeric gene joins exon 2 of the retinoic acid receptor alpha (RARA) gene in-frame to PML exons 4-8. Expression is targeted specifically to early myeloid-lineage cells by the promoter and 5' regulatory elements of the human cathepsin G gene.
  • mutations:
  • Insertion
  • synonyms:
  • RP2,
  • RP2,
  • HCG-RARalpha-PML transgene,
  • HCG-RARalpha-PML transgene
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

4 Publication categories

Trail: Allele