======= TEC =======
== Gene Information ==
* **Official Symbol**: TEC
* **Official Name**: tec protein tyrosine kinase
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=7006|7006]]
* **UniProt**: [[https://www.uniprot.org/uniprot/P42680|P42680]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=TEC&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20TEC|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/600583|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: N/A
* **UniProt Summary**: Non-receptor tyrosine kinase that contributes to signaling from many receptors and participates as a signal transducer in multiple downstream pathways, including regulation of the actin cytoskeleton. Plays a redundant role to ITK in regulation of the adaptive immune response. Regulates the development, function and differentiation of conventional T-cells and nonconventional NKT-cells. Required for TCR-dependent IL2 gene induction. Phosphorylates DOK1, one CD28-specific substrate, and contributes to CD28-signaling. Mediates signals that negatively regulate IL2RA expression induced by TCR cross-linking. Plays a redundant role to BTK in BCR-signaling for B-cell development and activation, especially by phosphorylating STAP1, a BCR-signaling protein. Required in mast cells for efficient cytokine production. Involved in both growth and differentiation mechanisms of myeloid cells through activation by the granulocyte colony-stimulating factor CSF3, a critical cytokine to promoting the growth, differentiation, and functional activation of myeloid cells. Participates in platelet signaling downstream of integrin activation. Cooperates with JAK2 through reciprocal phosphorylation to mediate cytokine-driven activation of FOS transcription. GRB10, a negative modifier of the FOS activation pathway, is another substrate of TEC. TEC is involved in G protein-coupled receptor- and integrin-mediated signalings in blood platelets. Plays a role in hepatocyte proliferation and liver regeneration and is involved in HGF-induced ERK signaling pathway. TEC regulates also FGF2 unconventional secretion (endoplasmic reticulum (ER)/Golgi-independent mechanism) under various physiological conditions through phosphorylation of FGF2 'Tyr-215'. May also be involved in the regulation of osteoclast differentiation. {ECO:0000269|PubMed:10518561, ECO:0000269|PubMed:19883687, ECO:0000269|PubMed:20230531, ECO:0000269|PubMed:9753425}.
|BTK|
|Pkinase Tyr|
|SH2|
|SH3 1|
|Pkinase|
|PH|
|regulation of platelet activation|
|peptidyl-tyrosine autophosphorylation|
|non-membrane spanning protein tyrosine kinase activity|
|tissue regeneration|
|regulation of blood coagulation|
|regulation of hemostasis|
|regulation of coagulation|
|integrin-mediated signaling pathway|
|phospholipid binding|
|B cell receptor signaling pathway|
|regulation of wound healing|
|peptidyl-tyrosine phosphorylation|
|peptidyl-tyrosine modification|
|regeneration|
|regulation of response to wounding|
|Fc-epsilon receptor signaling pathway|
|T cell receptor signaling pathway|
|positive regulation of peptidyl-tyrosine phosphorylation|
|protein autophosphorylation|
|Fc receptor signaling pathway|
|regulation of peptidyl-tyrosine phosphorylation|
|antigen receptor-mediated signaling pathway|
|cytoskeleton|
|developmental growth|
|growth|
|immune response-activating cell surface receptor signaling pathway|
|wound healing|
|immune response-regulating cell surface receptor signaling pathway|
|regulation of body fluid levels|
|immune response-activating signal transduction|
|response to wounding|
|immune response-regulating signaling pathway|
|adaptive immune response|
|activation of immune response|
|regulation of cell activation|
|cytokine-mediated signaling pathway|
|positive regulation of immune response|
|peptidyl-amino acid modification|
|protein phosphorylation|
|cellular response to cytokine stimulus|
|positive regulation of protein phosphorylation|
|positive regulation of phosphorylation|
|regulation of response to external stimulus|
|response to cytokine|
|positive regulation of phosphorus metabolic process|
|positive regulation of phosphate metabolic process|
|regulation of immune response|
|positive regulation of immune system process|
|positive regulation of protein modification process|
|phosphorylation|
|regulation of protein phosphorylation|
|regulation of response to stress|
|ATP binding|
|regulation of phosphorylation|
|positive regulation of cellular protein metabolic process|
|regulation of immune system process|
|intracellular signal transduction|
|positive regulation of protein metabolic process|
|tissue development|
|regulation of phosphate metabolic process|
|regulation of phosphorus metabolic process|
|regulation of protein modification process|
|immune response|
\\
=== CRISPR Data ===
^Screen^Score^
|[[:results:exp289|Hydroxyurea 15μM R06 exp289]]|-1.98|
|[[:results:exp143|Phenformin 20μM R03 exp143]]|-1.71|
No correlation found to any other genes in chemogenomics.
Global Fraction of Cell Lines Where Essential: 0/739
^Tissue^Fraction Of Cell Lines Where Essential^
|1290807.0|0/1|
|909776.0|0/1|
|bile duct|0/28|
|blood|0/28|
|bone|0/26|
|breast|0/33|
|central nervous system|0/56|
|cervix|0/4|
|colorectal|0/17|
|esophagus|0/13|
|fibroblast|0/1|
|gastric|0/16|
|kidney|0/21|
|liver|0/20|
|lung|0/75|
|lymphocyte|0/16|
|ovary|0/26|
|pancreas|0/24|
|peripheral nervous system|0/16|
|plasma cell|0/15|
|prostate|0/1|
|skin|0/24|
|soft tissue|0/9|
|thyroid|0/2|
|upper aerodigestive|0/22|
|urinary tract|0/29|
|uterus|0/5|
== Essentiality in NALM6 ==
* **Essentiality Rank**: 16836
* **Expression level (log2 read counts)**: 2.99
{{:chemogenomics:nalm6 dist.png?nolink |}}