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Allele : Rho<tm5.1(RHO*/GFP)Jhw> rhodopsin; targeted mutation 5.1, John H Wilson

Primary Identifier  MGI:5702734 Allele Type  Targeted
Attribute String  Humanized sequence, Inserted expressed sequence, Null/knockout, Reporter Gene  Rho
Transmission  Germline Strain of Origin  129S7/SvEvBrd-Hprt1<b-m2>
Is Recombinase  false Is Wild Type  false
molecularNote  The endogenous gene was replaced with a floxed HPRT minigene and a human RHO gene fused to GFP via homologous recombination. The human RHO gene contains a C to T nonsense mutation resulting in a premature stop codon at amino acid position 344 (Q344X). Cre mediated recombination removed the minigene. The loxP site in the 5' UTR of the human gene reduces expression about 5 fold by interfering with mRNA translation.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Q344X-hRho-GFP,
  • Q344X-hRho-GFP
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1 Feature

Trail: Allele

Genome

1 Expresses

Trail: Allele

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

6 Publication categories

Trail: Allele