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Mybtm2.2Epr
Targeted Allele Detail
Summary
Symbol: Mybtm2.2Epr
Name: myeloblastosis oncogene; targeted mutation 2.2, E Premkumar Reddy
MGI ID: MGI:4457094
Synonyms: c-mybdelta, p89-
Gene: Myb  Location: Chr10:21000834-21036883 bp, - strand  Genetic Position: Chr10, 9.75 cM
Alliance: Mybtm2.2Epr page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:160189
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Modified isoform(s))
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsCre mediated recombination removed exon 9A. The absence of p89 protein expression was confirmed by western blot analysis on thymocyte extracts. (J:160189)
Generation of the Mybtm2.1Epr and Mybtm2.2Epr alleles
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Myb Mutation:  53 strains or lines available
References
Original:  J:160189 Baker SJ, et al., p89c-Myb is not required for fetal or adult hematopoiesis. Genesis. 2010 May;48(5):309-16
All:  1 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)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory