About   Help   FAQ
Ctsgtm2.1(PML/RARA)Ley
Targeted Allele Detail
Summary
Symbol: Ctsgtm2.1(PML/RARA)Ley
Name: cathepsin G; targeted mutation 2.1, Timothy J Ley
MGI ID: MGI:3526413
Synonyms: Ctsgtm2.1Ley, mCGPML-RARalpha, mCGPR(deltaPGK-neo), PRWT
Gene: Ctsg  Location: Chr14:56337342-56340031 bp, - strand  Genetic Position: Chr14, 28.19 cM
Alliance: Ctsgtm2.1(PML/RARA)Ley page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:84230
Parent Cell Line:  RW-4 (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Humanized sequence, Inserted expressed sequence)
Mutation:    Insertion
 
Ctsgtm2.1(PML/RARA)Ley expresses 2 genes
 
Mutation detailsA human cDNA encoding the PML-RARalpha fusion and a loxP flanked PGK-neo was inserted into the 5' UTR. Transient Cre expression removed the floxed PGK-neo. (J:84230)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
Loading...
Tumor Data
List all tumor models in MMHCdb carrying Ctsgtm2.1(PML/RARA)Ley
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Ctsg Mutation:  13 strains or lines available
References
Original:  J:84230 Westervelt P, et al., High-penetrance mouse model of acute promyelocytic leukemia with very low levels of PML-RARalpha expression. Blood. 2003 Sep 1;102(5):1857-65
All:  17 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory