nur38 Gene Detail

Summary

• Symbol
  nur38
• Name
  neurological 38
• Synonyms
  nur^m38Jus

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:3038395
• 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
  1 phenotype from 1 allele in 1 genetic background
  1 phenotype reference
  

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

Homozygous mice exhibit shaky movement.

References

• Summaries
  All 1

  Phenotypes 1
• Earliest
  J:89098 The Mouse Genome Project at The Baylor College of Medicine, Heritable mouse mutants from the Mouse Mutagenesis for Developmental Defects Program. MGI Direct Data Submission. 2004-5;