Opn1mwtm1(OPN1LW)Nat
Targeted Allele Detail
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Symbol: |
Opn1mwtm1(OPN1LW)Nat |
Name: |
opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan); targeted mutation 1, Jeremy Nathans |
MGI ID: |
MGI:2678763 |
Synonyms: |
Opn1mwR, Opn1mwred, R |
Gene: |
Opn1mw Location: ChrX:73171072-73194362 bp, + strand Genetic Position: ChrX, Syntenic
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Alliance: |
Opn1mwtm1(OPN1LW)Nat page
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Germline Transmission: |
Earliest citation of germline transmission:
J:85849
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
129
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Allele Type: |
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Targeted (Humanized sequence, Inserted expressed sequence) |
Mutations: |
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Insertion, Intragenic deletion
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Opn1mwtm1(OPN1LW)Nat expresses
1 gene
Knock-in expresses:
Organism |
Expressed Gene |
Homolog in Mouse |
Note |
human |
OPN1LW (5956) |
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Opn1mwtm1(OPN1LW)Nat expression driven by
1 gene
Knock-in expression driven by:
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Mutation details: 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.
(J:85849)
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View phenotypes and curated references for all genotypes (concatenated display).
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Original: |
J:85849 Smallwood PM, et al., Genetically engineered mice with an additional class of cone photoreceptors: implications for the evolution of color vision. Proc Natl Acad Sci U S A. 2003 Sep 30;100(20):11706-11 |
All: |
18 reference(s) |
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