Human Disease and Mouse Model Detail
|
Human Disease
|
Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency
OMIM ID: 613204
|
|
Synonyms
|
Myopathy, Congenital, Due to Integrin Alpha-7 Deficiency
|
|
View all models
|
View ALL (1) mouse models for this human disease.
|
Genes and
mouse models
|
Mutations in human and/or mouse homologs are associated with this disease
| |
|
|
*Gene is associated with the disease in this species |
| |
|
|
  | | |
Itga7*
|
ITGA7*
|
View 1 model
|
1:1 Homology
|
|
Mouse Models
Human Disease Modeled: Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency
Associated Mouse Gene:
Itga7
Analysis Tools