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Phenotypes Associated with This Genotype
Genotype
MGI:4940495
Allelic
Composition
Cd44tm1Hbg/Cd44tm1Hbg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd44tm1Hbg mutation (4 available); any Cd44 mutation (74 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• trend towards decreased osteoclast surface in distal femur at the age of 17 weeks
• increased neutrophil and macrophage density in the infarcted myocardium after 24 h of reperfusion
• higher neutrophil and macrophage density after 72 h and 7 days of reperfusion
• increased neutrophil accumulation in the lungs without compromising the control of bacterial growth
• neutrophils are prominent within alveoli and small conducting airways and bronchoalveolar lavages fluid, compared with the wild-type controls at day 20 after aerosol infection with low-dose M. tuberculosis
• lesions are more loosely organized than those from the wild-type group
• at day 30 postinfection, focal lesions begin to coalesce
• at day 65 postinfection, lesions are more severe and necrosis is greater than the wild-type

limbs/digits/tail
• greater proximal tibia and cortical thickness
• trend towards greater cortical area
• smaller medullary area
• shorter tibias

integument
• a significant delay in barrier recovery kinetics at 1 hour after acute barrier disruption
• reduced secretion of lamellar material and delayed post-secretory dispersion of secreted lamellar material at stratum granulosum-stratum corneum (SG-SC) junction of epidermis at 1 hour after acute barrier disruption
• aberrant apical polarity of LB secretion towards the SG-SC interface
• redistributed from apical to basolateral membranes
• reduced density of epidermal lamellar body (LB) in the cytosol of keratinocytes
• thinning of the epidermis
• loss of the rete ridges
• flattening of the epidermal-dermal interface
• decreased epidermal proliferation

homeostasis/metabolism
• enhanced and prolonged neutrophil and macrophage infiltration in the infarct in comparison with wild-type (WT) animals
• decreased myofibroblast infiltration and reduced collagen deposition in the healing infarct
• slightly reduced percentage of apoptotic cells in comparison with WT mice after 72 h of reperfusion
• normal percentage of apoptotic cells after 24 h of reperfusion
• attenuated proliferative response in comparison to WT cardiac fibroblasts
• increased left ventricular end-diastolic volume and a trend toward lower left ventricular mass in comparison with WT animals after 7 days of reperfusion
• a significant delay in barrier recovery kinetics at 1 hour after acute barrier disruption
• reduced secretion of lamellar material and delayed post-secretory dispersion of secreted lamellar material at stratum granulosum-stratum corneum (SG-SC) junction of epidermis at 1 hour after acute barrier disruption
• aberrant apical polarity of LB secretion towards the SG-SC interface
• redistributed from apical to basolateral membranes
• decreased total non-saponifiable lipid level in epidermis
• decreased cholesterol level in epidermis
• decreased myofibroblast infiltration and reduced collagen deposition in the healing infarct
• slightly reduced percentage of apoptotic cells in comparison with WT mice after 72 h of reperfusion
• lower myofibroblast density in the infarcted myocardium after 3 days of reperfusion
• reduced proliferative activity in the infarcted myocardium
• reduced collagen content in the infarct compared with WT mice after 7 days of reperfusion

skeleton
• trend towards decreased osteoclast surface in distal femur at the age of 17 weeks
• greater proximal tibia and cortical thickness
• trend towards greater cortical area
• smaller medullary area
• shorter tibias

hematopoietic system
• trend towards decreased osteoclast surface in distal femur at the age of 17 weeks

cardiovascular system
• enhanced and prolonged neutrophil and macrophage infiltration in the infarct in comparison with wild-type (WT) animals
• decreased myofibroblast infiltration and reduced collagen deposition in the healing infarct
• slightly reduced percentage of apoptotic cells in comparison with WT mice after 72 h of reperfusion
• normal percentage of apoptotic cells after 24 h of reperfusion
• attenuated proliferative response in comparison to WT cardiac fibroblasts
• increased left ventricular end-diastolic volume and a trend toward lower left ventricular mass in comparison with WT animals after 7 days of reperfusion

cellular
• trend towards decreased osteoclast surface in distal femur at the age of 17 weeks


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
01/06/2026
MGI 6.24
The Jackson Laboratory