Human Disease and Mouse Model Detail
|
Human Disease
|
Cutis Laxa, Autosomal Recessive, Type IIA; ARCL2A
OMIM ID: 219200
|
|
Synonyms
|
Arcl2;
Cutis Laxa with Bone Dystrophy;
Cutis Laxa with Congenital Disorder of Glycosylation;
Cutis Laxa with Growth and Developmental Delay;
Cutis Laxa with Joint Laxity and Retarded Development;
Cutis Laxa, Debre Type
|
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 |
| |
|
|
 | | |
Atp6v0a2
|
ATP6V0A2*
|
|
1:1 Homology
|
|
Analysis Tools