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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Eno2-Ighmbp2)17Cx
transgene insertion 17, Gregory A Cox
MGI:3765055
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Ighmbp2nmd-2J/Ighmbp2nmd-2J
Tg(Eno2-Ighmbp2)17Cx/?
involves: C57BL/6J * C57BLKS/J MGI:3765069
cx2
Ighmbp2nmd-2J/Ighmbp2nmd-2J
Tg(Eno2-Ighmbp2)17Cx/?
Tg(Ttn-Ighmbp2)108Cx/?
involves: C57BL/6J * C57BLKS/J MGI:3785245
cx3
Ighmbp2nmd-2J/Ighmbp2nmd-2J
Tg(Eno2-Ighmbp2)17Cx/?
Tg(Ttn-Ighmbp2)45Cx/?
involves: C57BL/6J * C57BLKS/J MGI:3785263


Genotype
MGI:3765069
cx1
Allelic
Composition
Ighmbp2nmd-2J/Ighmbp2nmd-2J
Tg(Eno2-Ighmbp2)17Cx/?
Genetic
Background
involves: C57BL/6J * C57BLKS/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ighmbp2nmd-2J mutation (5 available); any Ighmbp2 mutation (46 available)
Tg(Eno2-Ighmbp2)17Cx mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at 49 days for males and 54 days for females
• maximum life span is 87 days for females

cardiovascular system
• grossly dilated hearts with one or more thrombi
• prolonged P-R interval
• sometimes split

muscle
N
• grossly normal hind limb muscle phenotype
• grossly dilated hearts with one or more thrombi
• mild myopathic changes including myocyte degeneration and regeneration with centralized nucleii

nervous system
N
• axon morphology and nerve root diameters are normal

respiratory system
• consolidation of lungs
• reduced breathing rate (bradypnea)

growth/size/body

homeostasis/metabolism
• 3-7 days prior to clearly evident clinical signs of heart disease, total plasma CK and cardiac-specific CK-MB levels in 5- to 9-week-old mice become significantly elevated
• consolidation of lungs




Genotype
MGI:3785245
cx2
Allelic
Composition
Ighmbp2nmd-2J/Ighmbp2nmd-2J
Tg(Eno2-Ighmbp2)17Cx/?
Tg(Ttn-Ighmbp2)108Cx/?
Genetic
Background
involves: C57BL/6J * C57BLKS/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ighmbp2nmd-2J mutation (5 available); any Ighmbp2 mutation (46 available)
Tg(Eno2-Ighmbp2)17Cx mutation (1 available)
Tg(Ttn-Ighmbp2)108Cx mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• increased heart weight proportionally distributed throughout all 4 chambers, but aside from this the presence of both transgenes rescues nmd-2J homozygotes to a wild-type phenotype including no cardiomyopathy

growth/size/body
• increased heart weight proportionally distributed throughout all 4 chambers, but aside from this the presence of both transgenes rescues nmd-2J homozygotes to a wild-type phenotype including no cardiomyopathy




Genotype
MGI:3785263
cx3
Allelic
Composition
Ighmbp2nmd-2J/Ighmbp2nmd-2J
Tg(Eno2-Ighmbp2)17Cx/?
Tg(Ttn-Ighmbp2)45Cx/?
Genetic
Background
involves: C57BL/6J * C57BLKS/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ighmbp2nmd-2J mutation (5 available); any Ighmbp2 mutation (46 available)
Tg(Eno2-Ighmbp2)17Cx mutation (1 available)
Tg(Ttn-Ighmbp2)45Cx mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• increased heart weight proportionally distributed throughout all 4 chambers, but aside from this the presence of both transgenes rescues nmd-2J homozygotes to a wild-type phenotype including no cardiomyopathy

growth/size/body
• increased heart weight proportionally distributed throughout all 4 chambers, but aside from this the presence of both transgenes rescues nmd-2J homozygotes to a wild-type phenotype including no cardiomyopathy





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory