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Del(11Mpo-Chad)18Brd Cytogenetic Marker Detail
Summary
  • Symbol
    Del(11Mpo-Chad)18Brd
  • Name
    deletion, Chr 11, Bradley 18
  • Synonyms
    Del18Brd
  • Feature Type
    cytogenetic marker
  • IDs
    MGI:3653212
Location & Maps
more
  • Genetic Map
    Chromosome 11, Syntenic
  • Mapping Data
    1 experiment
Human Diseases
more
  • Diseases
    2 with Del(11Mpo-Chad)18Brd mouse models

Human Disease Mouse Models
       Tetralogy of Fallot; TOF   OMIM: 187500 View 1 model
Transposition of the Great Arteries, Dextro-Looped 1; DTGA1   OMIM: 608808 View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    10 phenotypes from 1 allele in 1 genetic background
    1 phenotype reference
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryogenesis
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
tumorigenesis
vision/eye

Click cells to view annotations.
  • All Mutations and Alleles
    1
  • Targeted
    1
Polymorphisms
less
  • SNPs within 2kb
    57931 from dbSNP Build 137
References
more
  • Summaries
    All 2
    Diseases 1
    Phenotypes 1
  • Earliest
    J:109163 Yu YE, et al., A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice. Genetics. 2006 May;173(1):297-307

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
02/02/2016
MGI 6.02
The Jackson Laboratory