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Phenotypes Associated with This Genotype
Genotype
MGI:3033578
Allelic
Composition
Timp1tm1Pds/Timp1tm1Pds
Genetic
Background
involves: 129S4/SvJae
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Timp1tm1Pds mutation (1 available); any Timp1 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• indistinguishable from wild-type controls in metastasis assays

growth/size/body
N
• body weight equivalent to control mice at same age

reproductive system
N
• histologically normal ovaries
• number of healthy and atretic follicles equivalent to those in control mice
• serum estradiol concentrations equivalent to control mice
• ovary weight equivalent to control mice
• exhibit a significantly greater number of endometrial glands at P15 and P20; however, by P25, the number of glands is similar to wild-type, indicating accelerated endometrial gland formation
• accelerated endometrial gland formation during early postnatal uterine development
• mice that displayed normal estrus had uteri weighing significantly more than wild-type controls during estrus (J:64154)
• exhibit an increase in uterine wet weight at P5, P10 and P25 (J:96729)
• decreased length of estrus period or failure to display estrus
• longer periods of proestrus
• less than 50% exhibited normal estrus cycle
• ~50% achieved pregnancy vs. 78% in wild-type controls
• those that did become pregnant produced fewer litters over a 12-month period than wild-type controls
• when litters were produced, fewer pups per litter were born

cardiovascular system
• homozygotes form significantly larger aneurysms than wild-type after elastase infusion to induce aneurysm formation (to model abdominal aortic aneurysm) (J:101938)
• homozygotes, unlike wild-type, also develop aneurysms following saline injection (J:101938)
• homozygotes show increased and continued progression of aneurysm formation compared with wild-type in a thoracic aortic aneurysm model (induced by calcium chloride treatment) (J:102182)
• increased left ventricle end-diastolic pressure and volume vs. wild-type controls
• exhibit accelerated myocardial remodeling after myocardial infarction (coronary ligation) as indicated by increased left ventricular (LV) dilatation and LV dysfunction the accelerated remodeling can be rescued by MMP inhibition

immune system
• bacterial clearance following corneal infection is increased with 2 to 3 orders of magnitude fewer viable bacteria being found in mutant eyes 24 - 48 hours after infection

hematopoietic system
N
• normal blood cell counts and subtype distribution
• bone marrow cellularity is decreased by approximately 50% without changes in subtype composition

homeostasis/metabolism
• exhibit accelerated myocardial remodeling after myocardial infarction (coronary ligation) as indicated by increased left ventricular (LV) dilatation and LV dysfunction the accelerated remodeling can be rescued by MMP inhibition
• during estrus and diestrus

endocrine/exocrine glands
• exhibit a significantly greater number of endometrial glands at P15 and P20; however, by P25, the number of glands is similar to wild-type, indicating accelerated endometrial gland formation


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)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory