rs61879341
This variant is located in the ANO5 gene.
▶ClinVar annotation
Uncertain Significance★★★☆
3 submitters1 publicationnot provided; Limb-girdle muscular dystrophy, recessive; Miyoshi myopathy; ANO5-Related Muscle Diseases
View on ClinVar →About ANO5
This gene encodes a member of the anoctamin family of transmembrane proteins. The encoded protein is likely a calcium activated chloride channel. Mutations in this gene have been associated with gnathodiaphyseal dysplasia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2009]
View all ANO5 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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