stm Gene Detail

Summary

• Symbol
  stm
• Name
  stumpy

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:98434
  NCBI Gene: 20882
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome Unknown

Mutations,
Alleles, and
Phenotypes

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

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

Mutations in this gene affect cartilage-formed bones resulting dwarfism.

Sequences &
Gene Models

• NCBI Gene
  20882

Other
Accession IDs

MGD-MRK-14626

References

• Summaries
  All 9

  Phenotypes 6
• Earliest
  J:5848 Johnson DR, Ultrastructural observations on stumpy (stm), a new chondrodystrophic mutant in the mouse. J Embryol Exp Morphol. 1977 Jun;39(1):279-84
• Latest
  J:132820 Town T, et al., The stumpy gene is required for mammalian ciliogenesis. Proc Natl Acad Sci U S A. 2008 Feb 26;105(8):2853-8