ANXA11 Gene

Last updated on: 30.04.2023

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DefinitionThis section has been translated automatically.

The ANXA11 gene (ANXA11 stands for Annexin A11) is a protein-coding gene located on chromosome 10q22.3. The ANXA11 gene encodes a member of the annexin family, a group of calcium-dependent phospholipid-binding proteins.

General informationThis section has been translated automatically.

Annexins have unique N-terminal domains and conserved C-terminal domains that contain calcium-dependent phospholipid binding sites. The encoded AnnexinA11 protein acts as an antigen recognized by sera from patients with various autoimmune diseases. It binds specifically to calcyclin in a calcium-dependent manner. Several transcript variants encoding two distinct isoforms have been identified.

Diseases associated with ANXA11 include amyotrophic lateral sclerosis (Nahm M et al. 2020). Associations with sarcoidosis have also been reported (Zhou H et al. 2016).

LiteratureThis section has been translated automatically.

  1. Nahm M et al (2020) ANXA11 mutations in ALS cause dysregulation of calcium homeostasis and stress granule dynamics. Sci Transl Med 12:eaax3993.
  2. Zhou H et al. (2016) The Association between ANXA11 Gene Polymorphisms and Sarcoidosis: a Meta-Analysis and systematic review. Sarcoidosis Vasc Diffuse Lung Dis 33:102-11.

Last updated on: 30.04.2023