Automated description from the Alliance of Genome Resources (Release 7.4.0)
Predicted to enable intracellularly calcium-gated chloride channel activity. Predicted to be involved in chloride transmembrane transport and plasma membrane repair. Located in vesicle. Is expressed in several structures, including heart; limb; musculoskeletal system; perichondrium; and somite. Used to study autosomal recessive limb-girdle muscular dystrophy type 2L and gnathodiaphyseal dysplasia. Human ortholog(s) of this gene implicated in Miyoshi muscular dystrophy 3; autosomal recessive limb-girdle muscular dystrophy type 2L; gnathodiaphyseal dysplasia; and isolated elevated serum creatine phosphokinase levels. Orthologous to human ANO5 (anoctamin 5).
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