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Mapping Data
Experiment
  • Experiment
    TEXT-Physical Mapping
  • Chromosome
    5
  • Reference
    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
  • ID
    MGI:1929443
Genes
GeneAlleleAssay TypeDescription
Eif4h direct sequencing 303e12
Lat2 direct sequencing 303e12
Rfc2 direct sequencing 303e12
Clip2 direct sequencing 303e12
Notes
  • Experiment
    The authors sequenced the BAC containing the Wbscr15 gene and compared the sequence to data obtained from the sequencing of the human syntenic region. A percent identity plot (PIP) between the mouse and human genomic regions revealed the presence of the Cyln2, Rfc2, Wbscr5 and Wbscr1 genes on the BAC. The order and orientation of the genes on Chromosome 5 was determined to be: centromere - 5' - Wbscr1 - 3' (~4.0kb) - 5' - Lat2 - 3' (~1.5kb) - 3' - Rfc2 - 5'.

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
11/12/2024
MGI 6.24
The Jackson Laboratory