Symbol Name ID |
Itga7
integrin alpha 7 MGI:102700 |
Darker colors indicate more annotations |
Human Phenotypes | Torticollis |
Achilles tendon contracture |
Knee flexion contracture |
Calf muscle hypertrophy |
Calf muscle pseudohypertrophy |
Flexion contracture |
Hamstring contractures |
Hypotonia |
Difficulty climbing stairs |
Muscle weakness |
Gowers sign |
Respiratory insufficiency due to muscle weakness |
Increased variability in muscle fiber diameter |
Skeletal muscle atrophy |
Fatty replacement of skeletal muscle |
Muscular dystrophy |
Disease(s) Associated with ITGA7 | ||||||||||||||||
congenital muscular dystrophy due to integrin alpha-7 deficiency | ||||||||||||||||
Duchenne muscular dystrophy |
Mouse Phenotypes | abnormal vascular smooth muscle morphology |
vascular smooth muscle hyperplasia |
vascular smooth muscle hypertrophy |
skeletal muscle necrosis |
abnormal soleus morphology |
skeletal muscle fiber atrophy |
increased skeletal muscle fiber size |
increased variability of skeletal muscle fiber size |
centrally nucleated skeletal muscle fibers |
abnormal skeletal muscle morphology |
abnormal diaphragm morphology |
abnormal skeletal muscle fiber type ratio |
dystrophic muscle |
muscle degeneration |
abnormal muscle physiology |
myopathy |
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Availability | Mouse Genotype | ||||||||||||||||
Itga7tm1Burk/Itga7tm1Burk | |||||||||||||||||
Itga7tm1Umr/Itga7tm1Umr |
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 05/14/2024 MGI 6.23 |
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