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Del(9Apoa1-Apoa4)1Hmez Cytogenetic Marker Detail
Summary
  • Symbol
    Del(9Apoa1-Apoa4)1Hmez
  • Name
    deletion, Chr 9, Hafid Mezdour 1
  • Feature Type
    chromosomal deletion
  • IDs
    MGI:5582320
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 9, Syntenic
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    5 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.
References
more
  • Summaries
    All 1
    Phenotypes 1
  • Earliest
    J:109005 Mezdour H, et al., Characterization of a new mouse model for human apolipoprotein A-I/C-III/A-IV deficiency. J Lipid Res. 2006 May;47(5):912-20

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
11/19/2024
MGI 6.24
The Jackson Laboratory