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Allele : Opn1mw<tm1(OPN1LW)Nat> opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan); targeted mutation 1, Jeremy Nathans

Primary Identifier  MGI:2678763 Allele Type  Targeted
Attribute String  Humanized sequence, Inserted expressed sequence Gene  Opn1mw
Transmission  Germline Strain of Origin  129
Is Recombinase  false Is Wild Type  false
molecularNote  Human cDNA encoding OPN1LW was inserted at the endogenous mouse Opn1mw locus, replacing a 3' portion of exon 2 and all of exons 3, 4, and 5. The allele putatively produces a hybrid protein consisting of 92 N-terminal residues encoded by mouse exon 1 and the 5' portion of exon 2, and 266 C-terminal residues encoded by the human cDNA. Nearly the entire chromophore binding pocket, as well as the residues that account for the difference in absorbance spectra between human and mouse, is derived from the human sequence. Immunostaining indicated expression of the hybrid protein and electroretinogram indicated that the spectral sensitivity of cones containing the targeted allele was similar to that of human red cones.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • R,
  • Opn1mw<R>,
  • Opn1mw<R>,
  • Opn1mw<red>,
  • R,
  • Opn1mw<red>
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1 Feature

Trail: Allele

Genome

1 Expresses

Trail: Allele

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

1 Driven By

Trail: Allele

21 Publication categories

Trail: Allele