Human Disease and Mouse Model Detail
|
Human Disease
|
Spinocerebellar Ataxia 5; SCA5
OMIM ID: 600224
|
|
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 |
| |
|
|
  | | |
Sptbn2*
|
SPTBN2*
|
View 1 model
|
1:1 Homology
|
|
Mouse Models
Human Disease Modeled: Spinocerebellar Ataxia 5; SCA5
Associated Mouse Gene:
Sptbn2
NOT Models
No similarity to the expected human disease phenotype was found.
Analysis Tools