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Mapping Data
Experiment
  • Experiment
    TEXT-Genetic Cross
  • Chromosome
    10
  • Reference
    J:36348 Guay-Woodford LM, et al., Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. Kidney Int. 1996 Oct;50(4):1158-65
  • ID
    MGI:47877
Genes
GeneAlleleAssay TypeDescription
Bicc1 Bicc1jcpk-bpk visible phenotype
Notes
  • Reference
    Authors map bpk in close vicinity to jcpk but state that they are currently unable to determine whether the jcpk phenotype results from disruptions in the same locus as bpk or whether it involves two closely linked genes, one of which is bpk.
  • Experiment
    An end-mapping strategy was applied to localize Bicc1. Chromosomal haplotypes generated by typing only markers at the ends of each chromosome of ((BALB/c - +/bpk) x CAST/Ei)F1 intercross mutant progeny indicated linage to mouse Chromosome 10. These progenypresented a significant paucity of the apparently non-recombinant CAST/Ei (wild type) haplotype on this 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
12/10/2024
MGI 6.24
The Jackson Laboratory