Del(10Prmt2-Pdxk)4Yey Cytogenetic Marker Detail

Summary

• Symbol
  Del(10Prmt2-Pdxk)4Yey
• Name
  deletion, Chr 10, Y Eugene Yu 4
• Synonyms
  Del(10Prmt2-Pdxk)1Yey

• Feature Type
  chromosomal deletion
• IDs
  MGI:4818366

Location &
Maps

• Sequence Map
  Chr10:76043060-78300782 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 10, Syntenic
• Mapping Data
  1 experiment

Human Diseases

• Diseases
  1 with Del(10Prmt2-Pdxk)4Yey mouse models

Human Disease

Mouse Models

chromosomal deletion syndrome

IDs

chromosomal deletion syndrome      

DOID:0060388

View 1 model

Mouse Models

Human Disease Modeled: chromosomal deletion syndrome

Allelic Composition	Genetic Background	Reference	Phenotypes
Del(10Prmt2-Pdxk)4Yey/+	129S/SvEv-Del(10Prmt2-Pdxk)129S/SvEv-Del(10Prmt2-Pdxk)4Yey	J:161398	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
  4 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

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

Mice heterozygous for this deletion exhibit impaired spatial learning and contextual conditioning.

References

• Summaries
  All 2

  Diseases 1

  Phenotypes 1
• Earliest
  J:161398 Yu T, et al., Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice. Mamm Genome. 2010 Jun;21(5-6):258-67