This transgene consists of a fusion protein containing the N-terminal globular head domain and long central coiled-coil motif of NUMA1, including the oligomerization domain, and the C-terminus, domains C-F, of RARA, including the ATRA-binding site, RA-dependent DNA-binding site, and retinoid X receptor alpha and nuclear corepressor/coactivator interfaces, under the control of the human cathepsin G promoter. This fusion protein results from a translocation t(11:17)(q13;q21) associated with human cases of acute promyelocytic leukemia. The CTSG promoter drives expression in immature cells of the neutrophil lineage. RT-PCR indicates transgene expression in multiple organs at 4.5 months of age. Two lines were made but no line numbers were specified. (J:88103)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
Not Specified
--
Insertion
--
2
--
3

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

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PMID
Journal
Year
IF
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