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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
Torticollis
Intellectual disability
Intellectual disability, mild
Obstructive sleep apnea
Hyporeflexia
Loss of ambulation
Tip-toe gait
Waddling gait
Motor delay
Delayed gross motor development
Disease(s) Associated with ITGA7
congenital muscular dystrophy due to integrin alpha-7 deficiency
Duchenne muscular dystrophy

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
04/23/2024
MGI 6.23
The Jackson Laboratory