Del(8A4-B3)7H Cytogenetic Marker Detail

Summary

• Symbol
  Del(8A4-B3)7H
• Name
  deletion, Chr8, Harwell 7
• Synonyms
  Del7H, Del(8)7H, Del(8)Chy-3 7H, Del(8Efha2-Myo9b)7H

• Feature Type
  chromosomal deletion
• IDs
  MGI:4430113
  NCBI Gene: 13328

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome 8, cytoband A4-B3

Human Diseases

• Diseases
  1 with Del(8A4-B3)7H mouse models

Human Disease

Mouse Models

hereditary lymphedema

IDs

hereditary lymphedema      

DOID:0050580
ICD9CM:757.0
OMIM:PS153100
ORDO:79452
UMLS_CUI:C1313885

View 1 model

Mouse Models

Human Disease Modeled: hereditary lymphedema

Allelic Composition	Genetic Background	Reference	Phenotypes
Del(8A4-B3)7H/+	involves: 101/H * C3H/HeH	J:209628	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
  8 phenotypes from 1 allele in 1 genetic background
  3 phenotype references
  

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

Sequences &
Gene Models

• NCBI Gene
  13328

Other
Accession IDs

MGD-MRK-25303, MGI:103981

References

• Summaries
  All 6

  Diseases 1

  Phenotypes 3
• Earliest
  J:3564 Cattanach BM, et al., Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouse. Nat Genet. 1993 Jan;3(1):56-61
• Latest
  J:209628 Brouillard P, et al., Genetics of lymphatic anomalies. J Clin Invest. 2014 Mar 3;124(3):898-904