M1616b Gene Detail

Summary

• Symbol
  M1616b
• Name
  mutant 1616b
• Synonyms
  line 1616

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:5515460
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 13, Syntenic

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  2 phenotypes from multigenic genotypes
  1 phenotype reference
  

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

Mice hemizygous for this mutation exhibit prenatal lethality and failure of chorion failure.

References

• Summaries
  All 2

  Phenotypes 1
• Earliest
  J:101156 Bogani D, et al., Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12477-82