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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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     ATP6V0A2* Atp6v0a2   HomoloGene and HGNC

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
MGI 6.03
The Jackson Laboratory