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Mapping Data
Experiment
  • Experiment
    TEXT-Physical Mapping
  • Chromosome
    3
  • Reference
    J:80336 Di Palma F, et al., Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14994-9
  • ID
    MGI:2652659
Genes
GeneAlleleAssay TypeDescription
D3Mit185 overlapping clones, direct sequencing, sequence analysis
D3Mit260 overlapping clones, direct sequencing, sequence analysis
Mcoln3 overlapping clones, direct sequencing, sequence analysis
Mcoln2 overlapping clones, direct sequencing, sequence analysis
Lpar3 overlapping clones, direct sequencing, sequence analysis
D3Mit292 overlapping clones, direct sequencing, sequence analysis
D3Mit259 overlapping clones, direct sequencing, sequence analysis
Notes
  • Experiment
    The authors constructed a physical map of the critical VaJ region spanning 350kb. Two overlapping BAC clones RP23-121J1 and RP23-108E10 were sequenced. Sequence analysis revealed the order of markers in the region as: D3Mit85 - D3Mit260 - 5'- Mcoln3 - 3'- 5'- Mcoln2-3' - 5'- Edg7 - 3' - D3Mit292 - D3Mit259 - telomere. Further analysis showed that mutations in Mcoln3 are responsible for the VaJ phenotype.

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
04/23/2024
MGI 6.23
The Jackson Laboratory