Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Mybtm1Ssp
Name:	myeloblastosis oncogene; targeted mutation 1, S Steven Potter
MGI ID:	MGI:2662859
Gene:	Myb  Location: Chr10:21000834-21036883 bp, - strand  Genetic Position: Chr10, 9.75 cM
Alliance:	Mybtm1Ssp page

Germline Transmission:	Earliest citation of germline transmission: J:43747
Parent Cell Line:	D3 (ES Cell)
Strain of Origin:	129S2/SvPas

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)

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:	54 assay results
In Structures Affected by this Mutation:	3 anatomical structure(s)

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:	53 strains or lines available

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:	27 reference(s)