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Allele : Otop1<ied> otopetrin 1; inner ear defect

Primary Identifier  MGI:4881519 Allele Type  Chemically induced (ENU)
Gene  Otop1 Inheritance Mode  Recessive
Strain of Origin  C3HeB/FeJ Is Recombinase  false
Is Wild Type  false
molecularNote  A T to A transversion was identified in the splicing donor site of exon 2. As a result of this change, splice varients a and b are absent. A modified splice variant c in which exon 1 is spliced directly to exon 3 rather than into exon 2, is found in the inner ear and testes.
  • 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

1 Carried By

Trail: Allele

0 Driven By

4 Publication categories

Trail: Allele