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Mapping Data
Experiment
  • Experiment
    TEXT-Cytogenetic Localization
  • Chromosome
    X
  • Reference
    J:10686 Keer JT, et al., Genetic mapping in the region of the mouse X-inactivation center. Genomics. 1990 Aug;7(4):566-72
  • ID
    MGI:41406
Genes
GeneAlleleAssay TypeDescription
Dmd visible phenotype
DXSmh120 Southern analysis DXSmh120
T(X;16)16H visible phenotype
Zfx Southern analysis pDP1068
Ar Southern analysis pMCVAR
Eda visible phenotype
DXCrc169 Southern analysis EM169
DXCrc28 Southern analysis EM28
DXCrc171 Southern analysis EM171
Taf1 Southern analysis CCG1
DXCrc13 Southern analysis EM13
DXSmh44 Southern analysis DXSmh44
Pgk1 reported elsewhere
Notes
  • Experiment
    Mouse x Chinese hamster somatic cell hybrid line B20c12 containing the proximal portion of the X Chromosome translocation T(X;16)H as the only mouse chromosome was used to map genes Dmd and DXSmh120 to this proximal segment. Mapping distal to this segment were loci Zfx, Ar, Ta, DXCrc169, DXCrc28, DXCrc171, Taf1, DXCrc13, DXSmh44 and Pgk1. The latter group of loci had previously been physically mapped proximal to the HD3 breakpoint, thus placing them in the distal third of band of D of Chromosome X.

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
12/10/2024
MGI 6.24
The Jackson Laboratory