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Allele : Pde6b<rd10> phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 10

Primary Identifier  MGI:2388259 Allele Type  Spontaneous
Gene  Pde6b Inheritance Mode  Recessive
Strain of Origin  CXB1/ByJ Is Recombinase  false
Is Wild Type  false
molecularNote  An initial complementation test with Pde6b rd1 demonstrated allelism. Sequence analysis shows that the rd10 mutation is caused by a missense mutation in exon 13, which encodes the beta subunit of the protein.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • Pde6b<rd1-J>,
  • rd10,
  • Pde6b<rd1-J>,
  • rd10
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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

158 Publication categories