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Symbol
Name
ID
Itga7
integrin alpha 7
MGI:102700
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Increased variability in muscle fiber diameter
Skeletal muscle atrophy
Fatty replacement of skeletal muscle
Congenital muscular dystrophy
Myopathy
Infantile muscular hypotonia
Neonatal hypotonia
Disease(s) Associated with ITGA7
congenital muscular dystrophy due to integrin alpha-7 deficiency

Mouse Phenotypes
abnormal vascular smooth muscle morphology
vascular smooth muscle hyperplasia
vascular smooth muscle hypertrophy
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 soleus morphology
abnormal skeletal muscle fiber type ratio
skeletal muscle necrosis
dystrophic muscle
muscle degeneration
abnormal muscle physiology
myopathy
Availability Mouse Genotype
Itga7tm1Burk/Itga7tm1Burk
Itga7tm1Umr/Itga7tm1Umr

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory