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Human Disease and Mouse Model Detail
Human Disease

Term: Cutis Laxa, Autosomal Recessive, Type IIA; ARCL2A
OMIM ID: 219200

Synonyms Arcl2; Cutis Laxa, Debre Type; 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
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Atp6v0a2 ATP6V0A2
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory