dde Gene Detail

Summary

• Symbol
  dde
• Name
  disproportionate dwarf and eye defect

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:4354223
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr1:70406398-76771320 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 1, Syntenic
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  15 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

homozygotes have shortened limbs, fused toes on the hindfeet, retinal dysplasia, and varying lifespans with some dying just past weaning. Males are sterile and female fertility is reduced.

References

• Summaries
  All 1

  Phenotypes 1
• Earliest
  J:159016 Harris BS, et al., Disproportionate dwarf and eye defect (dde): A new recessive mutation with eye defects has been found on Chromosome 1. MGI Direct Data Submission. 2010;