About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Trib2Tg(Thy1-Trh/APP*)2.1Ingm
transgene insertion 2.1, Ingenium Pharmaceuticals
MGI:5294354
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Trib2Tg(Thy1-Trh/APP*)2.1Ingm/Trib2Tg(Thy1-Trh/APP*)2.1Ingm involves: C57BL/6 * DBA/1 MGI:5294357
cx2
Qpcttm1.2Tbay/Qpcttm1.2Tbay
Trib2Tg(Thy1-Trh/APP*)2.1Ingm/Trib2Tg(Thy1-Trh/APP*)2.1Ingm
involves: 129S2/SvPas * C57BL/6J MGI:5294364
cx3
Qpctlm1Ingm/Qpctlm1Ingm
Trib2Tg(Thy1-Trh/APP*)2.1Ingm/Trib2Tg(Thy1-Trh/APP*)2.1Ingm
involves: C3HeB/FeJ MGI:5294365
cx4
Trib2Tg(Thy1-Trh/APP*)2.1Ingm/Trib2+
Tg(Thy1-APP*)2.2Ingm/0
involves: C57BL/6 * DBA/1 MGI:5294359


Genotype
MGI:5294357
hm1
Allelic
Composition
Trib2Tg(Thy1-Trh/APP*)2.1Ingm/Trib2Tg(Thy1-Trh/APP*)2.1Ingm
Genetic
Background
involves: C57BL/6 * DBA/1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trib2Tg(Thy1-Trh/APP*)2.1Ingm mutation (0 available); any Trib2 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• between 5 and 7 months of age often due to feeding difficulties

nervous system
• the amyloid beta load peaks at 7 months of age while the pyroglutamate amyloid beta load peaks at 4 weeks of age
• neuronal loss is seen at 3 months of age in the CA1 pyramidal cell layer
• loss of more than 40% of neurons in the rostral hippocampal CA1 region
• loss of almost 50% of pyramidal neurons in the CA1 pyramidal cell layer by 5 months of age
• loss of almost 50% of pyramidal neurons in the CA1 pyramidal cell layer by 5 months of age
• at 2 and 3 months of age
• reduced at 5 months of age
• progressive age dependent astrocytosis beginning at 2 months of age
• at 5 months of age
• dramatic loss detectable at P28

behavior/neurological
• onset of behavioral phenotypes at 4 weeks of age
• progressive decline in home cage free drinking behavior with age
• progressive decline in home cage free feeding behavior with age
• display cramping or tremors when lifted by the tail
• at 3 months of age
• performance on a rotarod is less than 20% that of wild-type controls
• abnormal posture and rigor at 3 months of age
• progressive decline with age

growth/size/body
• about 30% lower compared to wild-type controls at 4.5 months of age
• detectable at 4 weeks of age

hematopoietic system
• at 2 and 3 months of age
• reduced at 5 months of age

immune system
• at 2 and 3 months of age
• reduced at 5 months of age

homeostasis/metabolism
• the amyloid beta load peaks at 7 months of age while the pyroglutamate amyloid beta load peaks at 4 weeks of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Alzheimer's disease DOID:10652 J:176575




Genotype
MGI:5294364
cx2
Allelic
Composition
Qpcttm1.2Tbay/Qpcttm1.2Tbay
Trib2Tg(Thy1-Trh/APP*)2.1Ingm/Trib2Tg(Thy1-Trh/APP*)2.1Ingm
Genetic
Background
involves: 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Qpcttm1.2Tbay mutation (0 available); any Qpct mutation (8 available)
Trib2Tg(Thy1-Trh/APP*)2.1Ingm mutation (0 available); any Trib2 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the pyroglutamate amyloid beta load is reduced compared to transgenic mice wild-type for Qpct

homeostasis/metabolism
• the pyroglutamate amyloid beta load is reduced compared to transgenic mice wild-type for Qpct




Genotype
MGI:5294365
cx3
Allelic
Composition
Qpctlm1Ingm/Qpctlm1Ingm
Trib2Tg(Thy1-Trh/APP*)2.1Ingm/Trib2Tg(Thy1-Trh/APP*)2.1Ingm
Genetic
Background
involves: C3HeB/FeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Qpctlm1Ingm mutation (0 available); any Qpctl mutation (14 available)
Trib2Tg(Thy1-Trh/APP*)2.1Ingm mutation (0 available); any Trib2 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the pyroglutamate amyloid beta load is similar to transgenic mice wild-type for Qpctl

homeostasis/metabolism
• the pyroglutamate amyloid beta load is similar to transgenic mice wild-type for Qpctl




Genotype
MGI:5294359
cx4
Allelic
Composition
Trib2Tg(Thy1-Trh/APP*)2.1Ingm/Trib2+
Tg(Thy1-APP*)2.2Ingm/0
Genetic
Background
involves: C57BL/6 * DBA/1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Thy1-APP*)2.2Ingm mutation (0 available)
Trib2Tg(Thy1-Trh/APP*)2.1Ingm mutation (0 available); any Trib2 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• onset is later than in mice homozygous for Trib2Tg(Thy1-Trh/APP*)2.1Ingm
• neurodegeneration in the CA1 pyramidal cell layer
• onset is later than in mice homozygous for Trib2Tg(Thy1-Trh/APP*)2.1Ingm
• onset is later than in mice homozygous for Trib2Tg(Thy1-Trh/APP*)2.1Ingm

behavior/neurological
• delayed
• onset is later than in mice homozygous for Trib2Tg(Thy1-Trh/APP*)2.1Ingm
• display cramping or tremors when lifted by the tail
• onset is later than in mice homozygous for Trib2Tg(Thy1-Trh/APP*)2.1Ingm

growth/size/body
• onset is later than in mice homozygous for Trib2Tg(Thy1-Trh/APP*)2.1Ingm

hematopoietic system
• onset is later than in mice homozygous for Trib2Tg(Thy1-Trh/APP*)2.1Ingm

immune system
• onset is later than in mice homozygous for Trib2Tg(Thy1-Trh/APP*)2.1Ingm

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Alzheimer's disease DOID:10652 J:176575





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
12/10/2024
MGI 6.24
The Jackson Laboratory