Mapping Data

Experiment

• Experiment
  TEXT-Genetic Cross
• Chromosome
  19
• Reference
  J:50114 ul Haque MF, et al., Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse. Nat Genet. 1998 Oct;20(2):157-62
• ID
  MGI:1330578

Genes

Gene	Allele	Assay Type
D19Mit135		PCR amplified length variant
D19Mit13		PCR amplified length variant
Papss2	Papss2^bm	visible phenotype
D19Mit64		PCR amplified length variant

Notes

• Experiment
  In a predefined backcross the mouse bm phenotype segregated within a 0.7 cM genomic segment of mouse Chromosome 19 defined proximately by D19Mit135 and distally by D19Mit64 which includes the marker D19Mit13. D19Mit13 is non-recombinant with the bm phenotype. Further, BLAST analysis led to the identification of D19Mit13 sequences within an intron of Papss2.