Tim Gene Detail

Summary

• Symbol
  Tim
• Name
  translocation induced circling mutation

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:98751
  NCBI Gene: 107698
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 4, Syntenic

Mutations,
Alleles, and
Phenotypes

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

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

Mutations in this gene result in impaired motor coordination and corneal defects.

Expression

• cDNA Data
  1

Sequences &
Gene Models

• NCBI Gene
  107698

Molecular
Reagents

• All nucleic 1

  cDNA 1

Other
Accession IDs

MGD-MRK-15109

References

• Summaries
  All 5

  Phenotypes 2
• Earliest
  J:10392 Lewis SE, et al., A new dominant neurological mutant induced in the mouse by ethylene oxide. Mutat Res. 1990 Apr;229(2):135-9
• Latest
  J:315119 Inaguma Y, et al., Morphological characterization of mammalian timeless in the mouse brain development. Neurosci Res. 2015 Mar;92:21-8