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Human Disease and Mouse Model Detail
Human Disease Cutis Laxa, Autosomal Recessive, Type IIA; ARCL2A
OMIM ID: 219200
Synonyms Arcl2; Cutis Laxa; 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
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Atp6v0a2 ATP6V0A2*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/09/2014
MGI 5.20
The Jackson Laboratory