SCUBA

CARD11 — Caspase recruitment domain family member 11

CARD11 belongs to a gene co-expression module in 2 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

CARD11's module in each cell type

Cell typeModuleShares the module with
Hematopoietic progenitor cellsLymphocyte Signaling
Lymphcyte development
ADGRG5, AHR, AKNA, CORO1A, CYTH4, KIAA0930, LSP1, PAK1 +3 more
Mucosal-associated invariant T cellTCR Activation Signaling
TCR Signaling
ARFGEF1, ARIH1, CCDC88C, CD226, GLS, KANSL1, KMT5B, MAP3K2 +12 more

About the gene

SynonymsBIMP3, CARMA1
Chromosome7: 2906142-3044228
Predicted locationIntracellular
Essential geneNo
Protein classCancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins
Biological processImmunity

Function

Adapter protein that plays a key role in adaptive immune response by transducing the activation of NF-kappa-B downstream of T- cell receptor (TCR) and B-cell receptor (BCR) engagement. Transduces signals downstream TCR or BCR activation via the formation of a multiprotein complex together with BCL10 and MALT1 that induces NF-kappa-B and MAP kinase p38 (MAPK11, MAPK12, MAPK13 and/or MAPK14) pathways. Upon activation in response to TCR or BCR triggering, CARD11 homooligomerizes to form a nucleating helical template that recruits BCL10 via CARD-CARD interaction, thereby promoting polymerization of BCL10 and subsequent recruitment of MALT1: this leads to I-kappa-B kinase (IKK) phosphorylation and degradation, and release of NF-kappa-B proteins for nuclear translocation. Its binding to DPP4 induces T-cell proliferation and NF-kappa-B activation in a T-cell receptor/CD3-dependent manner. Promotes linear ubiquitination of BCL10 by promoting the targeting of BCL10 to RNF31/HOIP. Stimulates the phosphorylation of BCL10. Also activates the TORC1 signaling pathway.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.