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Clutm1Jakh
Targeted Allele Detail

Nomenclature
Symbol: Clutm1Jakh
Name: clusterin; targeted mutation 1, Judith A K Harmony
MGI ID: MGI:2181011
Gene: Clu   Location: Chr14:66587320-66600385 bp, + strand    Genetic Position: Chr14, 28.0 cM
Mutation
origin
Germline Transmission: Earliest citation of germline transmission: J:65660
Parent Cell Line: D3 (ES Cell)
Strain of Origin: 129S2/SvPas
Mutation
description
Allele Type: Targeted (knock-out)
Mutations: Insertion, Intragenic deletion
  An HPRT cassette replaced exons 1 and 2. Normal transcript was undetectable in homozygous mutant tissue. Western blot analysis of plasma and liver extracts showed an absence of protein in homozygous mutant mice. (J:2892, J:65660, J:67960)
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 Clu Mutation: 1 strain or line available
Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms

(show or hide all annotated terms)

Genotypes are listed in the next section.

      Key:  
hm homozygous ht heterozygous
cn conditional genotype  cx complex: > 1 genome feature
tg involves transgenes ot other: hemizygous, indeterminate,...
N normal phenotype expected model not found
Affected SystemsGenotypes:
 
hm1
 
hm2
 
tg3
 
tg4
  
cardiovascular system          
   
  
homeostasis/metabolism          
   
  
immune system          
   
  
muscle          
   
  
nervous system          
N 
  
other phenotype          
  
 
  
Disease Models          
  
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 hm1   
Clutm1Jakh/Clutm1Jakh involves: 129S2/SvPas
  
 hm2   
Clutm1Jakh/Clutm1Jakh involves: Black Swiss * FVB/N
  
 tg3   Disease Model  
Apoetm1Unc/Apoetm1Unc
Clutm1Jakh/Clutm1Jakh
Tg(APPV717F)109Ili/Tg(APPV717F)109Ili
involves: 129P2/OlaHsd * 129S2/SvPas
  
 tg4   Disease Model  
Clutm1Jakh/Clutm1Jakh
Tg(APPV717F)109Ili/Tg(APPV717F)109Ili
involves: 129S2/SvPas
Disease
models
Mouse Models
of Human Disease
NoteGenotypeRef(s)
 
Allelic Composition
Genetic Background
Models with phenotypic similarity to human diseases not associated with human CLU.
Alzheimer Disease; AD
OMIM ID: 104300
 
 
tg3
Apoetm1Unc/Apoetm1Unc
Clutm1Jakh/Clutm1Jakh
Tg(APPV717F)109Ili/Tg(APPV717F)109Ili
involves: 129P2/OlaHsd * 129S2/SvPasJ:107702
 
 
tg4
Clutm1Jakh/Clutm1Jakh
Tg(APPV717F)109Ili/Tg(APPV717F)109Ili
involves: 129S2/SvPasJ:78357
Models involving transgenes or other mutation types.1
Alzheimer Disease; AD
OMIM ID: 104300
 
 
tg3
Apoetm1Unc/Apoetm1Unc
Clutm1Jakh/Clutm1Jakh
Tg(APPV717F)109Ili/Tg(APPV717F)109Ili
involves: 129P2/OlaHsd * 129S2/SvPasJ:107702
 
 
tg4
Clutm1Jakh/Clutm1Jakh
Tg(APPV717F)109Ili/Tg(APPV717F)109Ili
involves: 129S2/SvPasJ:78357
1Models involving transgenes or other mutation types may also appear in other sections of the table.
References
Original: J:65660 McLaughlin L et al., "Apolipoprotein J/clusterin limits the severity of murine autoimmune myocarditis" J Clin Invest 2000 Nov;106(9):1105-13
All: 18 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/20/2009
MGI_4.31
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