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Symbol
Name
ID
Itga7
integrin alpha 7
MGI:102700
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Cognitive impairment
Intellectual disability
Motor delay
Disease(s) Associated with ITGA7
congenital muscular dystrophy due to integrin alpha-7 deficiency

Mouse Phenotypes
intracranial hemorrhage
abnormal Schwann cell physiology
Availability Mouse Genotype
Itga7tm1Burk/Itga7tm1Burk
Itga7tm1Umr/Itga7tm1Umr

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
03/24/2020
MGI 6.15
The Jackson Laboratory