wfd Gene Detail

Summary

• Symbol
  wfd
• Name
  wide-faced

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:1310006
  NCBI Gene: 22392
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome X, Syntenic
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  1 phenotype reference
  

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

Homozygous females and hemizygous males for this X-linked viable mutation exhibit craniofacial abnormalities.

Sequences &
Gene Models

• NCBI Gene
  22392

References

• Summaries
  All 2

  Phenotypes 1
• Earliest
  J:50325 Reed V, et al., Characterisation of X-linked developmental mutants with craniofacial abnormalities. 12th International Mouse Genome Conference 9/29/98 - 10/3/98, Garmisch-Pastenkerchen, Germany. 1998;:E24 (Abstr.)