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Mapping Data
Experiment
  • Experiment
    TEXT-Physical Mapping
  • Chromosome
    X
  • Reference
    J:63277 Naylor MJ, et al., Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindness. Genomics. 2000 Jun 15;66(3):324-7
  • ID
    MGI:1861166
Genes
GeneAlleleAssay TypeDescription
Syp PCR amplified length variant, Southern analysis Clone 334I19
Cacna1f Clone 334I19
Notes
  • Experiment
    BAC clone 334I19 from the RPCI-22 library was informative in mapping the 5' end of Syp within 15 kb of the 3' end of Cacna1f on the mouse X Chromosome.

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