About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory