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Del(16Cbr1-Fam3b)1Rhr Cytogenetic Marker Detail
Summary
  • Symbol
    Del(16Cbr1-Fam3b)1Rhr
  • Name
    deletion, Chr 16, R H Reeves 1
  • Synonyms
    Del(16Cbr1-ORF9)1Rhr, Del(16Mx2-Cbr1)1Rhr, Del1Rhr
  • Feature Type
    chromosomal deletion
  • IDs
    MGI:3487249
Location &
Maps
more
  • Sequence Map
    Chr16:93607837-97504936 bp
  • From MGI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 16, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    8 phenotypes from 1 allele in 1 genetic background
    3 phenotypes from multigenic genotypes
    6 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
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.
References
more
  • Summaries
    All 7
    Phenotypes 6
  • Earliest
    J:93223 Olson LE, et al., A chromosome 21 critical region does not cause specific down syndrome phenotypes. Science. 2004 Oct 22;306(5696):687-90
  • Latest
    J:224899 Jiang X, et al., Genetic dissection of the Down syndrome critical region. Hum Mol Genet. 2015 Nov 15;24(22):6540-51

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
06/30/2020
MGI 6.15
The Jackson Laboratory