rs564438778
This variant is located in the CLIC5 gene.
▶ClinVar annotation
Autosomal recessive nonsyndromic hearing loss 103; not provided; CLIC5-related disorder
View on ClinVar →About CLIC5
This gene encodes a member of the chloride intracellular channel (CLIC) family of chloride ion channels. The encoded protein associates with actin-based cytoskeletal structures and may play a role in multiple processes including hair cell stereocilia formation, myoblast proliferation and glomerular podocyte and endothelial cell maintenance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
View all CLIC5 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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