Del(19Poll-Dcpd)1Nmt Cytogenetic Marker Detail

Summary

• Symbol
  Del(19Poll-Dcpd)1Nmt
• Name
  deletion, Chr 19, Noboru Motoyama 1

• Feature Type
  chromosomal deletion
• IDs
  MGI:5583961

Location &
Maps

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

• Genetic Map
  Chromosome 19, Syntenic

Human Diseases

• Diseases
  1 with Del(19Poll-Dcpd)1Nmt mouse models

Human Disease

Mouse Models

primary ciliary dyskinesia

IDs

primary ciliary dyskinesia      

DOID:9562
DOID:2925
MESH:D002925
NCI:C84638
OMIM:PS244400
ORDO:244
UMLS_CUI:C0008780

View 1 model

Mouse Models

Human Disease Modeled: primary ciliary dyskinesia

Allelic Composition	Genetic Background	Reference	Phenotypes
Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt	involves: 129P2/OlaHsd	J:75779	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
  21 phenotypes from 1 allele in 1 genetic background
  3 phenotype references
  

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

References

• Summaries
  All 3

  Diseases 1

  Phenotypes 3
• Earliest
  J:75779 Kobayashi Y, et al., Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome. Mol Cell Biol. 2002 Apr;22(8):2769-76
• Latest
  J:220930 Shinohara K, et al., Two rotating cilia in the node cavity are sufficient to break left-right symmetry in the mouse embryo. Nat Commun. 2012;3:622