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Allele : Cldn9<nmf329> claudin 9; neuroscience mutagenesis facility, 329

Primary Identifier  MGI:3055084 Allele Type  Chemically induced (ENU)
Gene  Cldn9 Inheritance Mode  Recessive
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  This mutation was discovered in an ENU mutagenesis screen. A T-to-C single nucelotide substitution in codon 35 is predicted to change the 35th amino acid of the encoded protein from phenylalanine (Phe) to leucine (Leu), located in the first predicted extracellular loop. Immunohistochemistry experiments with a polyclonal antibody that recognizes the unique C-terminus of the protein showed that the mutant protein is expressed in a spatiotemporal manner similar to the normal protein.
  • mutations:
  • Single point mutation
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

4 Publication categories