Dpmy Gene Detail

Summary

• Symbol
  Dpmy
• Name
  deficient peripheral myelin

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:5696872
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome 10, Syntenic

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  6 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

• All Mutations and Alleles
  1
• Spontaneous
  1
• Find Mice (IMSR)
  1 strains or lines available

Mice heterozygous for a spontaneous allele exhibit whole body shaking, reduced fertility, peripheral demyelination, neurogenic muscle atrophy, and partial postnatal lethality.

References

• Summaries
  All 1

  Phenotypes 1
• Earliest
  J:226382 Karst SY, et al., The deficient peripheral myelin mutation. MGI Direct Data Submission. 2015;