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Akt2tm1.1Mbb
Targeted Allele Detail

Nomenclature
Symbol: Akt2tm1.1Mbb
Name: thymoma viral proto-oncogene 2; targeted mutation 1.1, Morris J Birnbaum
MGI ID: MGI:2158456
Synonyms: Akt2 KO, Akt2-
Gene: Akt2   Location: Chr7:28376571-28425845 bp, + strand    Genetic Position: Chr7, 6.5 cM, cytoband B1
Mutation
origin
Germline Transmission: Earliest citation of germline transmission: J:71491
Parent Cell Line: E14 (ES Cell)
Strain of Origin: 129P2/OlaHsd
Mutation
description
Allele Type: Targeted (knock-out)
Mutations: Insertion, Intragenic deletion
  This allele is a derivative of Akt2tm1Mbb. Cre-mediated recombination in vivo under the control of a 6 kb 5'-flanking sequence from the Pou3f4 gene excised the floxed exons 4 and 5 in the germline. The excision of exons 4 and 5 results in a frameshift mutation that would lead to a premature termination even if the remaining exon 3 were to splice to exon 6. Exon 5 encodes the lysine residue necessary for catalytic activity. Western blot analyses using a polyclonal antibody did not detect protein in liver, muscle, and isolated adipocytes from homozygous mice. (J:71491)
Find Mice (IMSR) Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation: Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Akt2 Mutation: 27 strains or lines 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
 
cx3
 
tg4
 
tg5
 
tg6
 
tg7
  
adipose tissue          
      
  
digestive/alimentary system          
      
  
endocrine/exocrine glands          
      
  
hematopoietic system          
     
  
homeostasis/metabolism          
      
  
immune system          
     
  
muscle          
      
  
tumorigenesis          
     
  
normal phenotype          
N N    
 
  
Disease Models          
      
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 hm1   
Akt2tm1.1Mbb/Akt2tm1.1Mbb involves: 129P2/OlaHsd
  
 hm2   Disease Model  
Akt2tm1.1Mbb/Akt2tm1.1Mbb involves: 129P2/OlaHsd * C57BL/6
  
 cx3   
Akt2tm1.1Mbb/Akt2tm1.1Mbb
Akt3tm1Mbb/Akt3tm1Mbb
involves: 129P2/OlaHsd
  
 tg4   
Akt2tm1.1Mbb/Akt2tm1.1Mbb
Tg(MMTV-Erbb2)NK1Mul/Tg(MMTV-Erbb2)NK1Mul
involves: 129 * C57BL/6 * FVB/N
  
 tg5   
Akt2tm1.1Mbb/Akt2tm1.1Mbb
Tg(MMTV-PyVT)634Mul/0
involves: 129 * C57BL/6 * FVB/N
  
 tg6   
Akt1tm1Pnt/Akt1tm1Pnt
Akt2tm1.1Mbb/Akt2tm1.1Mbb
Tg(Lck-cre)1Cwi/0
involves: 129P2/OlaHsd
  
 tg7   
Akt1tm1Pnt/Akt1tm1Pnt
Akt2tm1.1Mbb/Akt2tm1.1Mbb
Akt3tm1Mbb/Akt3tm1Mbb
Tg(Lck-cre)1Cwi/0
involves: 129P2/OlaHsd
Disease
models
Mouse Models
of Human Disease
NoteGenotypeRef(s)
 
Allelic Composition
Genetic Background
Models with phenotypic similarity to human diseases associated with human AKT2.
Diabetes Mellitus, Noninsulin-Dependent; NIDDM
OMIM ID: 125853
 
 
hm2
Akt2tm1.1Mbb/Akt2tm1.1Mbbinvolves: 129P2/OlaHsd * C57BL/6J:71491
References
Original: J:71491 Cho H et al., "Insulin resistance and a diabetes mellitus-like syndrome in mice lacking the protein kinase Akt2 (PKB beta)." Science 2001 Jun 1;292(5522):1728-31
All: 20 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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