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Tlr9M7Btlr
Chemically induced Allele Detail
Summary
Symbol: Tlr9M7Btlr
Name: toll-like receptor 9; mutation 7, Bruce Beutler
MGI ID: MGI:4838258
Synonyms: CpG11, Tlr9CpG11
Gene: Tlr9  Location: Chr9:106099797-106104075 bp, + strand  Genetic Position: Chr9, 57.46 cM
Alliance: Tlr9M7Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThis mutation, discovered in a screen of progeny of ethylnitrosourea (ENU) mutagenized mice for impaired responses to Toll-like receptor (TLR) ligands, has been identified as a T to C transition at nucleotide position 1181 of the transcript that is predicted to result in the replacement of serine by proline at amino acid position 359 of the protein (S359P), in the second leucine rich repeat. (J:165701)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Tlr9 Mutation:  66 strains or lines available
References
Original:  J:165701 Huang H, et al., CpG11 is an allele of Tlr9 and causes Tlr9 signaling defects. MGI Direct Data Submission. 2010;
All:  42 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
11/12/2024
MGI 6.24
The Jackson Laboratory