Del(11Mpo-Chad)18Brd Cytogenetic Marker Detail

Summary

• Symbol
  Del(11Mpo-Chad)18Brd
• Name
  deletion, Chr 11, Bradley 18
• Synonyms
  Del18Brd

• Feature Type
  chromosomal deletion
• IDs
  MGI:3653212

Location &
Maps

• Sequence Map
  Chr11:87684610-94459953 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 11, Syntenic
• Mapping Data
  1 experiment

Human Diseases

• Diseases
  2 with Del(11Mpo-Chad)18Brd mouse models

Human Disease

Mouse Models

dextro-looped transposition of the great arteries

IDs

dextro-looped transposition of the great arteries      

DOID:0060770
ICD10CM:Q20.3
OMIM:608808
ORDO:860

View 1 model

Mouse Models

Human Disease Modeled: dextro-looped transposition of the great arteries

Allelic Composition	Genetic Background	Reference	Phenotypes
Del(11Mpo-Chad)18Brd/+	involves: 129S7/SvEvBrd * C57BL/6	J:109163	View

tetralogy of Fallot

IDs

tetralogy of Fallot      

DOID:6419
ICD10CM:Q21.3
ICD9CM:745.2
MESH:D013771
NCI:C84505
OMIM:187500
UMLS_CUI:C0039685

View 1 model

Mouse Models

Human Disease Modeled: tetralogy of Fallot

Allelic Composition	Genetic Background	Reference	Phenotypes
Del(11Mpo-Chad)18Brd/+	involves: 129S7/SvEvBrd * C57BL/6	J:109163	View

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

• Phenotype Summary
  10 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

• All Mutations and Alleles
  1
• Targeted
  1
• Find Mice (IMSR)
  0 strains or lines available

References

• 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