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Allele : Clrn2<mpc169H> clarin 2; muta-ped-c3pde 169, Harwell
Primary Identifier  MGI:5792002 Allele Type  Chemically induced (ENU)
Attribute String  Null/knockout Gene  Clrn2
Inheritance Mode  Recessive Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  Harwell ENU Mutagenesis
molecularNote  ENU mutagenesis produced a non-synonymous G-to-A transition at nucleotide 11 (ENSMUST00000053250) to substitute tryptophan with a stop codon at position 4 (Trp4*).
  • mutations:
  • Single point mutation
  • synonyms:
  • Clrn2<clarinet>,
  • Clrn2<p.Trp4*>,
  • Clrn2<clarinet>,
  • Clrn2<p.Trp4*>
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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




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