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dblr Gene Detail
Summary
  • Symbol
    dblr
  • Name
    doubleridge
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:2384508
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr19:26305715-37234461 bp
    From MGI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 19, cytoband C
  • Mapping Data
    3 experiments
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    6 phenotypes from 1 allele in 1 genetic background
    9 phenotype references
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
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Homozygotes for a transgene-induced mutation exhibit an abnormally broad and flat apical ectodermal ridge leading to polydactyly and syndactyly of the forelimbs. Mutants often have kinked tails and microphthalmia or anophthalmia.
References
more
  • Summaries
    All 10
    Phenotypes 9
  • Earliest
    J:82633 Adamska M, et al., Doubleridge, a mouse mutant with defective compaction of the apical ectodermal ridge and normal dorsal-ventral patterning of the limb. Dev Biol. 2003 Mar 15;255(2):350-62
  • Latest
    J:339662 Sung EA, et al., Dickkopf1 Promotes Pulmonary Fibrosis upon Bleomycin-Induced Lung Injury. Am J Pathol. 2023 Sep;193(9):1130-1142

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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Funding Information
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory