Symbol Name ID |
Itga7
integrin alpha 7 MGI:102700 |
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 |
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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 04/23/2024 MGI 6.23 |
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