UNC13D Gene

Last updated on: 22.12.2023

Dieser Artikel auf Deutsch

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

DefinitionThis section has been translated automatically.

The UNC13D gene (UNC13D stands for: Unc-13 Homolog D) is a protein-coding gene located on chromosome 17q25.3.

General informationThis section has been translated automatically.

The encoded protein belongs to the UNC13 family and has a similar domain structure to other family members. However, the molecule lacks an N-terminal phorbol ester-binding C1 domain, which is present in other Munc13 proteins. The encoded protein plays a role in the exocytosis of cytotoxic granules in lymphocytes.

It is required for granule maturation as well as for granule docking and priming at the immunological synapse.

The UNC13D protein regulates the assembly of recycling and late endosomal structures, leading to the formation of an endosomal exocytic compartment that fuses with perforin-containing granules at the immunological synapse and licenses them for exocytosis.

It regulates Ca(2+)-dependent secretory lysosome exocytosis in mast cells.

Clinical pictureThis section has been translated automatically.

Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis type 3, a genetically heterogeneous, rare autosomal recessive immunodeficiency disorder. Related signaling pathways include the innate immune system and deregulation of Rab and Rab effector genes in bladder cancer. An important paralog of this gene is BAIAP3.

LiteratureThis section has been translated automatically.

  1. Canna SW et al (2020) Pediatric hemophagocytic lymphohistiocytosis. Blood 135:1332-1343.
  2. Yoon HS et al (2010) UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis. Haematologica 95:622-626.

Last updated on: 22.12.2023