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pBSMyb11 Probe Detail
Nucleotide
Probe/Clone
  • Name
    pBSMyb11
  • Sequence Type
    genomic
  • ID
    MGI:1194826
  • Region Covered
    includes exons 2-8, introns 2-7, 5' and 3' flank
  • Parent Clone
    lambda-MM1
  • Insert Site
    BamHI
  • Insert Size
    11.0kb
Source
  • Species
    mouse, laboratory
Genes
Myb myeloblastosis oncogene
Polymorphisms
J:56493 Alagramam KN, et al., Genetics. 1999 Aug;152(4):1691-9
Endonuclease Gene Allele Fragments Strains
TaqI Myb c 3.1 C3H/Rl-KitlSl-3R
s 4.4 M. spretus
References
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
J:56493 Alagramam KN, et al., A new mouse insertional mutation that causes sensorineural deafness and vestibular defects. Genetics. 1999 Aug;152(4):1691-9
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory