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391O16 Probe Detail
Nucleotide
Probe/Clone
  • Name
    391O16
  • Sequence Type
    genomic
  • ID
    MGI:1343880
  • Region Covered
    includes listed markers and flanking regions
  • Child Clones
  • Vector Type
    BAC
  • Insert Size
    180.0kb
Source
  • Species
    mouse, laboratory
  • Strain
    CITB-CJ7-B
Genes
Ncf1 neutrophil cytosolic factor 1
Gtf2i general transcription factor II I
119L04aR DNA segment, 119L04aR (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)
391O16F DNA segment, 391O16F (Research Genetics)
256O10R DNA segment, 256O10R (Research Genetics)
03B03F DNA segment, 03B03F (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
05/07/2024
MGI 6.23
The Jackson Laboratory