About   Help   FAQ
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 (47 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





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory