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Allele : Ctsb<tm1Jde> cathepsin B; targeted mutation 1, Jan Deussing

Primary Identifier  MGI:2182129 Allele Type  Targeted
Attribute String  Null/knockout Gene  Ctsb
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
description  in combination with Ctsltm1Cptr, double homozygous mutant have some similarities but distinct phenotypic characteristics compared to the human syndrome: neuronal ceroid lipofuscinoses (NLCs)
molecularNote  A neomycin selection cassette was inserted into a BglII site in exon 4. Northern blot analysis of total RNA showed a lack of transcript in homozygous mutant mice. An absence of protein in homozygous mutant mice was determined by Western blot analysis of kidney lysosomal protein extracts. The proteolytic activity of the endogenous protein was found to be absent using an assay involving liver lysosomal extracts obtained from of homozygous mutant mice and a fluorogenic substrate.
  • mutations:
  • Insertion
  • synonyms:
  • Cat B<->,
  • Ctsb<->,
  • Cat B<->,
  • CathB<->,
  • Ctsb<->,
  • CTSB<->,
  • CTSB<->,
  • CathB<->
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

8 Carried By

0 Driven By

81 Publication categories