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Mybtm1Ssp
Targeted Allele Detail
Nomenclature
Symbol: Mybtm1Ssp
Name: myeloblastosis oncogene; targeted mutation 1, S Steven Potter
MGI ID: MGI:2662859
Gene: Myb  Location: Chr10:21124936-21160905 bp, - strand  Genetic Position: Chr10, 9.75 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:43747
Parent Cell Line:  D3 (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Insertion
    The endogenous locus was disrupted by the insertion of a neomycin selection cassette into exon 6. (J:43747)
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 46 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Myb Mutation:  22 strains or lines available
References
Original:  J:43747 Mucenski ML, et al., A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis. Cell. 1991 May 17;65(4):677-89
All:  17 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/29/2016
MGI 6.06
The Jackson Laboratory