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Allele : Pde6b<rd1-3H> phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1, 3 Harwell
Primary Identifier  MGI:2178319 Allele Type  Chemically induced (ENU)
Gene  Pde6b Strain of Origin  (C3H/HeN x BALB/cAnN)F1
Is Recombinase  false Is Wild Type  false
molecularNote  A nonsense mutation in exon 9 (G1133A) caused a premature stop codon at the tryptophan at amino acid position 378.
  • mutations:
  • Single point mutation
  • synonyms:
  • Gena362,
  • Gena362,
  • GENA 362,
  • GENA 362
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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Trail: Allele

0 Driven By

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Trail: Allele




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