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Allele : Tlr9<m4Btlr> toll-like receptor 9; mutation 4, Bruce Beutler

Primary Identifier  MGI:3774140 Allele Type  Chemically induced (ENU)
Gene  Tlr9 Inheritance Mode  Other (see notes)
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false Project Collection  Beutler Mutagenetix
description  The inheritance of the mutant phenotype is probably semidominant, like that of other Tlr9 mutations; however, homozygous mutants have not been examined.
molecularNote  The mutant phenotype, discovered in an ENU mutagenesis screen for impaired response of peritoneal macrophages to Toll-like receptor (TLR) ligands, is due to a T-to-C transition at nucleotide position 1284 (Genbank Accession NM_031178) in the second of two exons. It results in replacement of leucine by proline at amino acid position 393 (L393P), the initial leucine in the fourteenth extracellular leucine-rich repeat of the receptor's ectodomain.
  • mutations:
  • Single point mutation
  • synonyms:
  • Tlr9<CpG5>,
  • unmethylated CpG-oligodeoxynucleotide unresponsive 5,
  • CpG5,
  • unmethylated CpG-oligodeoxynucleotide unresponsive 5,
  • Tlr9<CpG5>,
  • CpG5
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

3 Publication categories

Trail: Allele