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Symbol
Name
ID
Itga7
integrin alpha 7
MGI:102700
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Scoliosis
Disease(s) Associated with ITGA7
congenital muscular dystrophy due to integrin alpha-7 deficiency

Mouse Phenotypes
kyphosis
Availability Mouse Genotype
Itga7tm1Burk/Itga7tm1Burk

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
02/05/2019
MGI 6.13
The Jackson Laboratory