Del(13)36H Cytogenetic Marker Detail

Summary

• Symbol
  Del(13)36H
• Name
  deletion, Chr 13, Harwell 36
• Synonyms
  Del(13)Svea36H, Del36H, small with variable eye anomalies, Svea

• Feature Type
  chromosomal deletion
• IDs
  MGI:104137
  NCBI Gene: 13268

Location &
Maps

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

• Genetic Map
  Chromosome 13, cytoband A3.3-A5
• Mapping Data
  2 experiments

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  38 phenotypes from multigenic genotypes
  5 phenotype references
  

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

Sequences &
Gene Models

• NCBI Gene
  13268

Other
Accession IDs

MGD-MRK-19553, MGD-MRK-25459

References

• Summaries
  All 7

  Phenotypes 5
• Earliest
  J:71411 Arkell RM, et al., Genetic, physical, and phenotypic characterization of the Del(13)Svea36H mouse. Mamm Genome. 2001 Sep;12(9):687-94
• Latest
  J:141688 Goldsworthy M, et al., Role of the transcription factor sox4 in insulin secretion and impaired glucose tolerance. Diabetes. 2008 Aug;57(8):2234-44