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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tbc1d25Gt(IST10205D5)Tigm
gene trap IST10205D5, Texas A&M Institute for Genomic Medicine
MGI:3957652
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ot1
Tbc1d25Gt(IST10205D5)Tigm/Y involves: C57BL/6N MGI:6467953


Genotype
MGI:6467953
ot1
Allelic
Composition
Tbc1d25Gt(IST10205D5)Tigm/Y
Genetic
Background
involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbc1d25Gt(IST10205D5)Tigm mutation (1 available); any Tbc1d25 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• at 4 weeks after partial transverse aortic constriction (TAC), cross-sectional area of cardiomyocytes is significantly larger than that in wild-type controls
• at 4 weeks after partial TAC, heart is significantly larger than in wild-type controls
• at 4 weeks after partial TAC, mice show increased ratios of heart weight to body weight (HW/BW) and heart weight to tibia length (HW/TL) relative to wild-type controls
• at 4 weeks after partial TAC, mice exhibit exacerbated cardiac hypertrophy and significantly increased mRNA expression levels of hypertrophy markers (ANP, BNP and MYH7) relative to wild-type controls
• at 4 weeks after partial TAC, hearts exhibit more prominent interstitial and perivascular fibrosis with significantly increased left ventricular collagen volume and mRNA expression levels of fibrosis markers relative to wild-type hearts
• at 4 weeks after partial TAC, cardiac interstitial fibrosis is more prominent than in wild-type hearts
• at 4 weeks after partial TAC, fractional shortening % (FS%) is significantly lower than that in wild-type controls
• at 4 weeks after partial TAC, ejection fraction % (EF%) is significantly lower than that in wild-type controls
• at 4 weeks after partial TAC, mice exhibit increased cardiac hypertrophy (increased ratios of heart weight to body weight, lung weight to body weight and heart weight to tibia length, larger gross heart size and cross-sectional area of cardiomyocytes) and increased cardiac fibrosis and left ventricular end-diastolic and end-systolic diameter with decreased fractional shortening and ejection fraction relative to wild-type controls

growth/size/body
• at 4 weeks after partial TAC, heart is significantly larger than in wild-type controls
• at 4 weeks after partial TAC, mice show increased ratios of heart weight to body weight (HW/BW) and heart weight to tibia length (HW/TL) relative to wild-type controls
• at 4 weeks after partial TAC, mice exhibit exacerbated cardiac hypertrophy and significantly increased mRNA expression levels of hypertrophy markers (ANP, BNP and MYH7) relative to wild-type controls
• at 4 weeks after partial TAC, lung weight to body weight (LW/BW) ratio is higher than that in wild-type controls

homeostasis/metabolism
• at 4 weeks after partial TAC, mice exhibit increased cardiac hypertrophy (increased ratios of heart weight to body weight, lung weight to body weight and heart weight to tibia length, larger gross heart size and cross-sectional area of cardiomyocytes) and increased cardiac fibrosis and left ventricular end-diastolic and end-systolic diameter with decreased fractional shortening and ejection fraction relative to wild-type controls

muscle
• at 4 weeks after partial transverse aortic constriction (TAC), cross-sectional area of cardiomyocytes is significantly larger than that in wild-type controls
• at 4 weeks after partial TAC, fractional shortening % (FS%) is significantly lower than that in wild-type controls
• at 4 weeks after partial TAC, ejection fraction % (EF%) is significantly lower than that in wild-type controls

respiratory system
• at 4 weeks after partial TAC, lung weight to body weight (LW/BW) ratio is higher than that in wild-type controls

cellular
• at 4 weeks after partial TAC, cardiac interstitial fibrosis is more prominent than in wild-type hearts





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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
11/19/2024
MGI 6.24
The Jackson Laboratory