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567C18 Probe Detail
Nucleotide
Probe/Clone
  • Name
    567C18
  • Sequence Type
    genomic
  • ID
    MGI:1343878
  • Region Covered
    includes listed markers and flanking regions
  • Child Clone
  • Vector Type
    Cosmid
  • Insert Size
    160.0kb
Source
  • Species
    mouse, laboratory
  • Strain
    CITB-CJ7-B
Genes
Ncf1 neutrophil cytosolic factor 1
38B16F DNA segment, 38B16F (Research Genetics)
119L04F DNA segment, 119L04F (Research Genetics)
38B16R DNA segment, 38B16R (Research Genetics)
94B16F DNA segment, 94B16F (Research Genetics)
sWSS86 DNA segment, sWSS86 (Research Genetics)
133J02R DNA segment, 133J02R (Research Genetics)
349F04F DNA segment, 349F04F (Research Genetics)
391O16R DNA segment, 391O16R (Research Genetics)
03B03R DNA segment, 03B03R (Research Genetics)
92N10R DNA segment, 92N10R (Research Genetics)
567C18F DNA segment, 567C18F (Research Genetics)
335F15R DNA segment, 335F15R (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
05/14/2024
MGI 6.23
The Jackson Laboratory