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Nox3het-R96
Chemically induced Allele Detail
Summary
Symbol: Nox3het-R96
Name: NADPH oxidase 3; head tilt R96
MGI ID: MGI:3034161
Gene: Nox3  Location: Chr17:3685515-3746536 bp, - strand  Genetic Position: Chr17, 2.05 cM
Alliance: Nox3het-R96 page
Mutation
origin
Strain of Origin:  C3H
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThe mutation in the R96 mouse was identified as a T-to-A nonsense mutation at coding nucleotide position 381 (c.381T>A), changing tyrosine codon 127 to a stop codon (p.Y127*). The resulting protein, if produced, would be truncated, lacking most of the relevant feature of NADPH oxidases and would be non-functional. (J:89010)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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
Carrying any Nox3 Mutation:  38 strains or lines available
References
Original:  J:89010 Paffenholz R, et al., Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase. Genes Dev. 2004 Mar 1;18(5):486-91
All:  1 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
04/09/2024
MGI 6.23
The Jackson Laboratory