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Ask your administrator if you think this is wrong. ======= IBTK ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: IBTK * **<color #00a2e8>Official Name</color>**: inhibitor of Bruton tyrosine kinase * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=25998|25998]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9P2D0|Q9P2D0]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=IBTK&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20IBTK|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/606457|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: Bruton tyrosine kinase (BTK) is a protein tyrosine kinase that is expressed in B cells, macrophages, and neutrophils. The protein encoded by this gene binds to BTK and downregulates BTK's kinase activity. In addition, the encoded protein disrupts BTK-mediated calcium mobilization and negatively regulates the activation of nuclear factor-kappa-B-driven transcription. This gene has a pseudogene on chromosome 18. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]. * **<color #00a2e8>UniProt Summary</color>**: N/A <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |Ank 2| |BTB| |RCC1| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |protein tyrosine kinase inhibitor activity| |negative regulation of protein tyrosine kinase activity| |negative regulation of peptidyl-tyrosine phosphorylation| |release of sequestered calcium ion into cytosol| |negative regulation of sequestering of calcium ion| |calcium ion transmembrane import into cytosol| |calcium ion transport into cytosol| |cytosolic calcium ion transport| |regulation of protein tyrosine kinase activity| |regulation of sequestering of calcium ion| |calcium ion transmembrane transport| |negative regulation of protein kinase activity| |negative regulation of kinase activity| |calcium ion transport| |regulation of peptidyl-tyrosine phosphorylation| |negative regulation of transferase activity| |positive regulation of cytosolic calcium ion concentration| |divalent metal ion transport| |divalent inorganic cation transport| |regulation of cytosolic calcium ion concentration| |negative regulation of protein phosphorylation| |cellular calcium ion homeostasis| |negative regulation of phosphorylation| |calcium ion homeostasis| |protein kinase binding| |cellular divalent inorganic cation homeostasis| |divalent inorganic cation homeostasis| |cellular metal ion homeostasis| |negative regulation of phosphate metabolic process| |negative regulation of phosphorus metabolic process| |inorganic cation transmembrane transport| |negative regulation of protein modification process| |cation transmembrane transport| |metal ion homeostasis| |cellular cation homeostasis| |metal ion transport| |cellular ion homeostasis| |inorganic ion transmembrane transport| |cation homeostasis| |inorganic ion homeostasis| |cellular chemical homeostasis| |ion homeostasis| |negative regulation of catalytic activity| |regulation of protein kinase activity| |cation transport| |regulation of kinase activity| |cellular homeostasis| |ion transmembrane transport| |regulation of transferase activity| |negative regulation of cellular protein metabolic process| |negative regulation of protein metabolic process| |chemical homeostasis| |negative regulation of molecular function| |transmembrane transport| |ion transport| |regulation of protein phosphorylation| |regulation of phosphorylation| |homeostatic process| |regulation of phosphate metabolic process| |regulation of phosphorus metabolic process| |establishment of localization in cell| |regulation of protein modification process| |membrane| </modal> \\ === CRISPR Data === <button type='primary' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> ^Screen^Score^ |[[:results:exp421|VHL-ligand-1 20μM R07 exp421]]|-1.88| |[[:results:exp535|Trimetrexate 0.03μM R08 exp535]]|2.03| </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> 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| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 6808 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 6.67 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='IBTK Expression in NALM6 Cells: 6.67'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:36by 127.0.0.1