Gene

CLIC5

Species
Homo sapiens
Symbol
CLIC5
Name
chloride intracellular channel 5
Synonyms
  • chloride intracellular channel 5A
  • chloride intracellular channel protein 5
Biotype
protein coding gene
Automated Description
Predicted to enable chloride channel activity and oxidoreductase activity. Involved in chloride transport and sensory perception of sound. Located in Golgi apparatus and actin cytoskeleton. Implicated in autosomal recessive nonsyndromic deafness 103.
RGD Description
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]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR45476
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Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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Annotation details
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    Disease Associations

    Cases where the expected disease association was NOT found
    Cell color indicative of annotation volume
    No data available

    Alleles and Variants

    Allele/Variant Symbol
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      Transgenic Alleles

      Species
      (carrying the transgene)
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      Transgenic construct
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          GRCh38
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          Sequence Details

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          Expression

          Primary Sources
          None
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          CLIC5 molecule type
          Interactor gene
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            Genetic Interactions

            CLIC5 role
            CLIC5 genetic perturbation
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