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ApcMin
Chemically induced Allele Detail

Nomenclature
Symbol: ApcMin
Name: adenomatosis polyposis coli; multiple intestinal neoplasia
MGI ID: MGI:1856318
Synonyms: ApcΔ850, Apc-, Apcdelta850, Min, Min-
Gene: Apc   Location: Chr18:34380638-34479735 bp, + strand    Genetic Position: Chr18, 15.0 cM
Mutation
origin
Strain of Origin: C57BL/6J
Mutation
description
Allele Type: Chemically induced (ENU)
Mutation: Single point mutation
  A transversion point mutation that alters nucleotide 2549 from a T to an A. This converts codon 850 from one encoding a leucine to a stop codon. (J:830)
Inheritance: Dominant
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation: Mouse Strains: 5 strains available      Cell Lines: 0 lines available
Carrying any Apc Mutation: 46 strains or lines available
Expression
In Mice Carrying this Mutation: 15 assay results
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:
 
ht1
 
ht2
 
ht3
 
ht4
 
ht5
 
cn6
 
cn7
 
cx8
 
cx9
 
cx10
 
cx11
 
cx12
 
cx13
 
cx14
 
cx15
 
cx16
 
cx17
 
cx18
 
cx19
 
cx20
 
cx21
 
cx22
 
cx23
 
cx24
 
cx25
 
cx26
 
cx27
 
cx28
 
cx29
 
cx30
 
cx31
 
cx32
 
cx33
 
cx34
 
cx35
 
cx36
 
cx37
 
cx38
 
cx39
 
cx40
 
cx41
 
cx42
 
cx43
 
cx44
 
cx45
 
cx46
 
cx47
 
cx48
 
cx49
 
cx50
 
cx51
 
cx52
 
cx53
 
cx54
 
cx55
 
cx56
 
cx57
 
cx58
 
cx59
 
tg60
 
tg61
  
adipose tissue          
                             N                               
  
cellular          
                                                          
  
digestive/alimentary system          
                     N                    
  
endocrine/exocrine glands          
                                                        
  
growth/size          
      N                                                    
  
hematopoietic system          
                           N                             
  
homeostasis/metabolism          
                                                        
  
immune system          
                                                            
  
life span/aging          
                N  N         N                      
  
muscle          
                             N                               
  
reproductive system          
                                                           
  
skeleton          
                                                            
  
tumorigenesis          
N       
 
  
Disease Models          
                                                         
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 ht1   
ApcMin/Apc+ B6.Cg-Brca2tm1Mbn ApcMin
  
 ht2   
ApcMin/Apc+ involves: 129P2/OlaHsd * C57BL/6
  
 ht3   Disease Model  
ApcMin/Apc+ involves: AKR/J * C57BL/6J
  
 ht4   
ApcMin/Apc+ involves: C57BL/6 * C57BL/6J
  
 ht5   
ApcMin/Apc+ involves: C57BL/6J
  
 cn6   
ApcMin/Apc+
Dnmt3btm1Jae/Dnmt3btm1Jae
Tg(Fabp1-cre)1Jig/0
involves: 129 * C57BL/6 * C57BL/6J * FVB/N
  
 cn7   
ApcMin/Apc+
Erbb3tm1.1Dwt/Erbb3tm2.1Dwt
Tg(Vil-cre)997Gum/0
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL
  
 cx8   Disease Model  
ApcMin/Apc+
Brca2tm1Mbn/Brca2+
B6.Cg-Brca2tm1Mbn ApcMin