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Allele : Pde6b<rd1-1H> phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1, 1 Harwell
Primary Identifier  MGI:2178317 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 G to A transition in position 1 of the intron 18 splice donor site is predicted to eliminate correct splicing.
  • mutations:
  • Single point mutation
  • synonyms:
  • GENA 338,
  • GENA 338,
  • Gena338,
  • Gena338
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories





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