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dde Gene Detail
Summary
  • Symbol
    dde
  • Name
    disproportionate dwarf and eye defect
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:4354223
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr1:70406398-76771320 bp
    From MGI annotation of GRCm39
  • View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 1, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    15 phenotypes from 1 allele in 1 genetic background
    1 phenotype reference
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
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
more
  • 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;

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
11/23/2021
MGI 6.17
The Jackson Laboratory