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P510M19 Probe Detail
Nucleotide
Probe/Clone
  • Name
    P510M19
  • Sequence Type
    genomic
  • ID
    MGI:1343868
  • Region Covered
    includes listed markers and flanking regions
  • Vector Type
    PAC
  • Insert Size
    190.0kb
Source
  • Species
    mouse, laboratory
  • Strain
    129/Sv
Genes
303E12F DNA segment, 303E12F (Research Genetics)
502H20R DNA segment, 502H20R (Research Genetics)
358A17R DNA segment, 358A17R (Research Genetics)
304D23R DNA segment, 304D23R (Research Genetics)
94B16R DNA segment, 94B16R (Research Genetics)
133J02F DNA segment, 133J02F (Research Genetics)
349F04R DNA segment, 349F04R (Research Genetics)
92N10F DNA segment, 92N10F (Research Genetics)
504N12R DNA segment, 504N12R (Research Genetics)
335F15F DNA segment, 335F15F (Research Genetics)
References
J:55324 DeSilva U, et al., Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. Genome Res. 1999 May;9(5):428-36

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
05/07/2024
MGI 6.23
The Jackson Laboratory