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Tdrd7nmf166
Chemically induced Allele Detail
Summary
Symbol: Tdrd7nmf166
Name: tudor domain containing 7; neuroscience mutagenesis facility, 166
MGI ID: MGI:4943539
Synonyms: NMF166, Tdrd7glcr5, Tdrd7grm5
Gene: Tdrd7  Location: Chr4:45965334-46034761 bp, + strand  Genetic Position: Chr4, 24.48 cM
Alliance: Tdrd7nmf166 page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU induced a C to T nonsense mutation at position 2187 in the coding region resulting in glutamine to stop mutation at amino acid 723. Western blot analysis did not detect any protein expression in the eyes from homozygous mice indicating this is a null allele. (J:68708, J:169836)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 2 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 10 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Tdrd7 Mutation:  43 strains or lines available
References
Original:  J:87349 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2004-7;
All:  3 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
12/10/2024
MGI 6.24
The Jackson Laboratory