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303E12 Probe Detail
Nucleotide
Probe/Clone
  • Name
    303E12
  • Sequence Type
    genomic
  • ID
    MGI:1343859
  • Region Covered
    includes listed markers and flanking regions
  • Child Clones
  • Vector Type
    BAC
  • Insert Size
    161.85kb
Source
  • Library
    CITB CJ7B (J:55325)
  • Species
    mouse, laboratory
  • Strain
    129/Sv
Genes
Clip2 CAP-GLY domain containing linker protein 2
42J20F DNA segment, 42J20F (Research Genetics)
502H20F DNA segment, 502H20F (Research Genetics)
303E12F DNA segment, 303E12F (Research Genetics)
303E12R DNA segment, 303E12R (Research Genetics)
Eif4h eukaryotic translation initiation factor 4H
304D23F DNA segment, 304D23F (Research Genetics)
Rfc2 replication factor C (activator 1) 2
211N06R DNA segment, 211N06R (Research Genetics)
504N12F DNA segment, 504N12F (Research Genetics)
Lat2 linker for activation of T cells family, member 2
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
J:66919 Doyle JL, et al., Divergent human and mouse orthologs of a novel gene (WBSCR15/Wbscr15) reside within the genomic interval commonly deleted in Williams syndrome. Cytogenet Cell Genet. 2000;90(3-4):285-90
J:73830 DeSilva U, et al., Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome. Genome Res. 2002 Jan;12(1):3-15

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
11/19/2024
MGI 6.24
The Jackson Laboratory