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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Igbp1tm1Imku
targeted mutation 1, Nobuo Sakaguchi
MGI:2656093
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Igbp1tm1Imku/Y
Tg(Igbp1b-cre)1Imku/0
B6.Cg-Igbp1tm1Imku Tg(Igbp1b-cre)1Imku MGI:3623760
cn2
Cd19tm1(cre)Cgn/Cd19+
Igbp1tm1Imku/Y
involves: 129P2/OlaHsd MGI:3603798
cn3
Igbp1tm1Imku/Y
Tg(Lck-cre)I57Jxm/?
involves: 129P2/OlaHsd * ICR MGI:3603799


Genotype
MGI:3623760
cn1
Allelic
Composition
Igbp1tm1Imku/Y
Tg(Igbp1b-cre)1Imku/0
Genetic
Background
B6.Cg-Igbp1tm1Imku Tg(Igbp1b-cre)1Imku
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Igbp1tm1Imku mutation (0 available); any Igbp1 mutation (8 available)
Tg(Igbp1b-cre)1Imku mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• prolonged response latency compared to control mice
• in probe trials using a Morris water maze, mutant mice spend less time in the quadrant where the hidden platform had been located

nervous system
N
• brain morphology is similar to control mice




Genotype
MGI:3603798
cn2
Allelic
Composition
Cd19tm1(cre)Cgn/Cd19+
Igbp1tm1Imku/Y
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd19tm1(cre)Cgn mutation (11 available); any Cd19 mutation (56 available)
Igbp1tm1Imku mutation (0 available); any Igbp1 mutation (8 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• no somatic hypermutation takes place
• decreased B220+ cells but cells have a normal maturation phenotype
• decreased numbers involve IgM+ IgDhi
• CD23+IgM+ follicular cells in the spleen were reduced as were CD40+ cells
• reduced in numbers although normal numbers of pro B cells are present in bone marrow
• germinal center formation is impaired
• impaired proliferative responses, failure of G1/S transition
• stimulated antibody production is low
• T cell dependent antibody production more affected than T cell independent production

hematopoietic system
• no somatic hypermutation takes place
• decreased B220+ cells but cells have a normal maturation phenotype
• decreased numbers involve IgM+ IgDhi
• CD23+IgM+ follicular cells in the spleen were reduced as were CD40+ cells
• reduced in numbers although normal numbers of pro B cells are present in bone marrow
• germinal center formation is impaired
• impaired proliferative responses, failure of G1/S transition
• stimulated antibody production is low
• T cell dependent antibody production more affected than T cell independent production

cellular
• impaired proliferative responses, failure of G1/S transition




Genotype
MGI:3603799
cn3
Allelic
Composition
Igbp1tm1Imku/Y
Tg(Lck-cre)I57Jxm/?
Genetic
Background
involves: 129P2/OlaHsd * ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Igbp1tm1Imku mutation (0 available); any Igbp1 mutation (8 available)
Tg(Lck-cre)I57Jxm mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• largely lacking in double positive cells
• demarcation between cortex and medulla indistinct
• peripheral spleen T cells 30% of control levels
• thymocyte production only 4.3% normal
• few proliferating thymocytes
• double negative cells are proportionately higher but absolute numbers are reduced
• development blocked at DN3 stage

hematopoietic system
• largely lacking in double positive cells
• demarcation between cortex and medulla indistinct
• peripheral spleen T cells 30% of control levels
• thymocyte production only 4.3% normal
• few proliferating thymocytes
• double negative cells are proportionately higher but absolute numbers are reduced
• development blocked at DN3 stage

endocrine/exocrine glands
• largely lacking in double positive cells
• demarcation between cortex and medulla indistinct
• thymocyte production only 4.3% normal
• few proliferating thymocytes





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory