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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Appl2tm1.1Test
targeted mutation 1.1, Joseph Testa
MGI:5703918
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Appl2tm1.1Test/Appl2tm1.1Test Not Specified MGI:5766634
cx2
Appl1tm1.2Test/Appl1tm1.2Test
Appl2tm1.1Test/Appl2tm1.1Test
involves: 129X1/SvJ MGI:5766636


Genotype
MGI:5766634
hm1
Allelic
Composition
Appl2tm1.1Test/Appl2tm1.1Test
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Appl2tm1.1Test mutation (0 available); any Appl2 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
N
• at 8 weeks of age, mice exhibit normal numbers and % of lymphocytes, monocytes, neutrophils, eosinophils, and basophils relative to controls
• no pernicious anemia is observed, as WBC counts and spleen and liver size are normal
• hematocrit is significantly increased, esp. in female mice
• MCHC is significantly decreased, esp. in female mice
• MCV is significantly increased, esp. in female mice

cellular
• primary MEFs derived from E13.5 embryos exhibit decreased Akt activation upon stimulation with HGF; in contrast, FBS- or EGF-induced Akt activation is relatively normal
• in vivo, basal Akt activity is not significantly altered in stomach, liver or muscle tissues
• primary MEFs derived from E13.5 embryos exhibit reduced HGF-induced transmembrane migration and decreased movement in a wound-healing assay as well as markedly decreased HGF-triggered invasion in a matrigel assay
• in contrast, EGF-induced migration and invasion are normal




Genotype
MGI:5766636
cx2
Allelic
Composition
Appl1tm1.2Test/Appl1tm1.2Test
Appl2tm1.1Test/Appl2tm1.1Test
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Appl1tm1.2Test mutation (0 available); any Appl1 mutation (45 available)
Appl2tm1.1Test mutation (0 available); any Appl2 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• unexpectedly, mice are viable and show grossly normal postnatal growth and fertility, similar to single homozygotes

hematopoietic system
N
• at 8 weeks of age, mice exhibit normal numbers and % of lymphocytes, monocytes, neutrophils, eosinophils, and basophils relative to controls
• no pernicious anemia is observed, as WBC counts and spleen and liver size are normal
• T cell development and Pi3k-Akt signaling in thymic T cells are normal
• hematocrit is significantly increased, esp. in female mice
• MCHC is significantly decreased, esp. in female mice
• MCV is significantly increased, esp. in female mice

cellular
• primary MEFs derived from E13.5 embryos exhibit decreased Akt activation upon stimulation with HGF; in contrast, FBS- or EGF-induced Akt activation is relatively normal
• in vivo, basal Akt activity is not significantly altered in stomach, liver or muscle tissues
• primary MEFs derived from E13.5 embryos exhibit reduced HGF-induced transmembrane migration and decreased movement in a wound-healing assay as well as markedly decreased HGF-triggered invasion in a matrigel assay
• in contrast, EGF-induced migration and invasion are normal





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory