us Gene Detail

Summary

• Symbol
  us
• Name
  urogenital syndrome

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:98918
  NCBI Gene: 22277
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 2, Syntenic
• Mapping Data
  5 experiments

Mutations,
Alleles, and
Phenotypes

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

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

Homozygous mutants have abnormal axial skeleton and urogenital organs. Mutants show reduced viability, retarded growth, thin hair coat, head-shaking, and serious defects of kidney, skeleton and reproductive organs.

Sequences &
Gene Models

• NCBI Gene
  22277

Other
Accession IDs

MGD-MRK-15375

References

• Summaries
  All 4

  Phenotypes 2
• Earliest
  J:14466 Lane PW, et al., Urogenital syndrome (us): a developmental mutation on chromosome 2 of the mouse. Mamm Genome. 1993 Sep;4(9):481-4