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Allele : Pde6b<rd1-2J> phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1, 2 Jackson

Primary Identifier  MGI:2665102 Allele Type  Chemically induced (ENU)
Gene  Pde6b Inheritance Mode  Recessive
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  This mutation was shown by genetic complementation analysis to be an allele of Pde6b. Molecular sequence analysis showed that this mutation corresponds to a point mutation in exon 16.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • NMF137,
  • neuroscience mutagenesis facility, 137,
  • Pde6b<2J>,
  • neuroscience mutagenesis facility, 137,
  • Pde6b<2J>,
  • Pde6b<nmf137>,
  • NMF137,
  • nmf137,
  • Pde6b<nmf137>,
  • nmf137
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

15 Publication categories

Trail: Allele