Del(1)3H Cytogenetic Marker Detail

Summary

• Symbol
  Del(1)3H
• Name
  deletion, Chr 1, Harwell 3
• Synonyms
  Del(1)Pax3^Sp-r3H, Del3H, Pax3^Sp-r, retarded splotch, Sp-3H

• Feature Type
  chromosomal deletion
• IDs
  MGI:103583
  NCBI Gene: 13249

Location &
Maps

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

• Genetic Map
  Chromosome 1, cytoband C5
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  5 phenotypes from 1 allele in 1 genetic background
  5 phenotype references
  

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

Sequences &
Gene Models

• NCBI Gene
  13249

Other
Accession IDs

MGD-MRK-24904

References

• Summaries
  All 10

  Phenotypes 5
• Earliest
  J:2944 Epstein DJ, et al., Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3. Cell. 1991 Nov 15;67(4):767-74
• Latest
  J:41878 Zoltewicz JS, et al., oto is a homeotic locus with a role in anteroposterior development that is partially redundant with Lim1. Development. 1999 Nov;126(22):5085-95