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Allele : Ltbp3<m1Btlr> latent transforming growth factor beta binding protein 3; mutation 1, Bruce Beutler

Primary Identifier  MGI:3723580 Allele Type  Chemically induced (ENU)
Gene  Ltbp3 Inheritance Mode  Recessive
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false Project Collection  Beutler Mutagenetix
molecularNote  This mutation, discovered because of its obvious homozygous phenotype among progeny of ENU-mutagenized mice, comprises a T-to-C transition at nucleotide position 2343 in exon 9 of the gene (GenBank Accession NM_008520) that results in the Cys452Arg amino acid substitution. Cys452 resides in the predicted 4th domain of the protein, which contains twelve EGF-like repeats and two 8-Cys motifs/TGF-bp repeats; the first of the latter (which is the third 8-Cys motif of the protein) is involved in disulfide bonding with inactive transforming growth factor, beta 1.
  • mutations:
  • Single point mutation
  • synonyms:
  • craniofacial and skeletal malformation with paralysis,
  • CSP,
  • craniofacial and skeletal malformation with paralysis,
  • Ltbp3<csp>,
  • Ltbp3<csp>,
  • CSP
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

0 Driven By

4 Publication categories