BLNK — B cell linker
BLNK belongs to a gene co-expression module in 3 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.
BLNK's module in each cell type
| Cell type | Module | Shares the module with | |
|---|---|---|---|
| Enterocytes | Long-gene nuclear transcripts Technical artifact | ARL15, CERS6, EXT1, FHIT, FUT8, KANK1, LDLRAD4, LRBA +6 more | View in SCUBA |
| Fibroblasts | Adventitial Fibroblast State Developmental | AKAP7, C1QA, CACNA1G, CALCRL, COL21A1, CYP1B1, FAT3, KIRREL2 +9 more | View in SCUBA |
| Hematopoietic progenitor cells | Dendritic Cell Progenitor Myeloid development | CCDC50, CD180, CLEC4A, HDAC9, HERPUD1, IRF8, LY86, NCF1 +1 more |
About the gene
| Synonyms | BASH, bca, BLNK-s, Ly57, SLP-65, SLP65 |
|---|---|
| Chromosome | 10: 96189171-96271587 |
| Predicted location | Intracellular |
| Essential gene | No |
| Protein class | Disease related genes, Human disease related genes, Predicted intracellular proteins |
| Biological process | B-cell activation |
Function
Functions as a central linker protein, downstream of the B- cell receptor (BCR), bridging the SYK kinase to a multitude of signaling pathways and regulating biological outcomes of B-cell function and development. Plays a role in the activation of ERK/EPHB2, MAP kinase p38 and JNK. Modulates AP1 activation. Important for the activation of NF-kappa-B and NFAT. Plays an important role in BCR- mediated PLCG1 and PLCG2 activation and Ca(2+) mobilization and is required for trafficking of the BCR to late endosomes. However, does not seem to be required for pre-BCR-mediated activation of MAP kinase and phosphatidyl-inositol 3 (PI3) kinase signaling. May be required for the RAC1-JNK pathway. Plays a critical role in orchestrating the pro-B cell to pre-B cell transition. May play an important role in BCR- induced B-cell apoptosis.
Human Protein Atlas · Open Targets · UniProt
Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.