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Dp(1)22H Cytogenetic Marker Detail
Summary
  • Symbol
    Dp(1)22H
  • Name
    duplication, Chr 1, Harwell 22
  • Synonyms
    Mut1171
  • Feature Type
    chromosomal duplication
  • IDs
    MGI:5466685
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 1, Syntenic
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 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
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.
Mice homozygous for this duplication exhibit growth retardation. Homozygosity apparently is embryonic lethal pre-implantation.
References
more
  • Summaries
    All 2
    Phenotypes 1
  • Earliest
    J:192801 Cattanach BM, et al., A further large Chr 1 duplication. Mouse Genome. 1997;95(2):486
  • Latest
    J:169366 MouseBookTM, Information obtained from MouseBookTM, Medical Research Council Mammalian Genetics Unit, Harwell, UK. Unpublished. 2005-2013;

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
11/12/2024
MGI 6.24
The Jackson Laboratory