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Tg(RHO-P23H)DTpd
Transgene Detail
Summary
Symbol: Tg(RHO-P23H)DTpd
Name: transgene insertion D, Thaddeus P Dryja
MGI ID: MGI:2181671
Synonyms: P23H-D
Transgene: Tg(RHO-P23H)DTpd  Location: unknown  
Alliance: Tg(RHO-P23H)DTpd page
Transgene
origin
Strain of Origin:  (C57BL/6 x DBA/2)F1
Transgene
description
Transgene Type:    Transgenic (Humanized sequence, Inserted expressed sequence)
Mutation:    Insertion
 
Tg(RHO-P23H)DTpd expresses 1 gene
 
Mutation detailsThe entire coding region of mutant human rhodopsin (P23H) implicated in dominantly inherited retinitis pigmentosa was used for the transgene. The transgene includes 4.2 kb of upstream sequence and 8.4 kb of downstream sequence. (J:76722)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Notes
Mutant lines D, E, and L harboring the mutant human rhodopsin gene were constructed. Lines D and E express 3x and 1x the amount of endogenous rhodopsin, respectively, resulting in severe retinitis pigmentosa. Line L expresses 1/6x the amount of endogenous rhodopsin and exhibits a mild disease phenotype.
References
Original:  J:76722 Olsson JE, et al., Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa. Neuron. 1992 Nov;9(5):815-30
All:  4 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory