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Allele : Otog<vbd> otogelin; vestibular balance defect

Primary Identifier  MGI:5883222 Allele Type  Chemically induced (ENU)
Attribute String  Not Specified Gene  Otog
Inheritance Mode  Recessive Strain of Origin  C3HeB/FeJ
Is Recombinase  false Is Wild Type  false
molecularNote  This ENU-induced mutation was isolated in the Munich genome wide ENU recessive mutagenesis program. Gene mapping identified a one base pair substitution, a T36351 to C36351 transition at the splice donor site of intron 29, leading to a frame-shift of translation inducing an addition of 16 new amino acids at the carboxyl-terminus and a premature stop codon.
  • mutations:
  • Single point mutation
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories

Trail: Allele