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Allele : Opn1sw<tm1Pugh> opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan); targeted mutation 1, Edward Pugh

Primary Identifier  MGI:5431111 Allele Type  Targeted
Gene  Opn1sw Transmission  Germline
Strain of Origin  129S6/SvEvTac Is Recombinase  false
Is Wild Type  false
molecularNote  Exon 1 was replaced with one in which an A to T transition results in the amino acid substitution of tyrosine for phenylalanine at position 81 (F81Y). An FRT-flanked neo cassette was inserted downstream of exon 3. qRT-PCR confirmed a 1000-fold reduction in transcript expression.
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • Opn1sw<Neo>,
  • Opn1sw<Neo>
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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

6 Publication categories