BTK
ENSG00000010671
Target class
Kinase
Chromosome
X
Approved drugs
8
Clinical candidates (approved and in development)
23
- Approved drugs
- 8
- ClinGen gene-disease validity
- Definitive
- Clinical candidates (approved and in development)
- 23
- Chemical probe available
- Yes
- Target name
- BTK
- Gene name
- Bruton tyrosine kinase
- Gene symbol
- BTK
- Protein name
- Tyrosine-protein kinase BTK (EC 2.7.10.2) (Agammaglobulinemia tyrosine kinase) (ATK) (B-cell progenitor kinase) (BPK) (Bruton tyrosine kinase)
- ATK
- XLA
- PSCTK1
- AGMX1
- IMD1
- Gene biotype
- Protein coding
- Gene family
- Pleckstrin homology domain containing|SH2 domain containing|Tec family tyrosine kinases
- Target class
- Kinase
- Target type
- Human gene
- Tissues expressed in
- 34
- Protein localisation evidence grade
- Supported
- Highest tissue expression
- 114
- Tissue specificity (Gini)
- 0.741
- Tissue specificity (tau)
- 0.967
- KEGG gene identifiers
- hsa:695
- Protein interaction confidence
- 0.8607
- Protein interaction partners
- 70
- R-HSA-1236974
- R-HSA-166058
- R-HSA-2029482
- R-HSA-2424491
- R-HSA-2871809
- R-HSA-416476
- R-HSA-416482
- R-HSA-5602498
- R-HSA-5603041
- R-HSA-5663213
- R-HSA-8964315
- R-HSA-9664422
- R-HSA-9679191
- R-HSA-983695
- End position
- 101390796
- Start position
- 101349338
- Chromosome
- X
- Strand
- Reverse
- Cytoplasm . Cell membrane
- Peripheral membrane protein . Nucleus . Membrane raft . Note=In steady state, BTK is predominantly cytosolic. Following B-cell receptor (BCR) engagement by antigen, translocates to the plasma membrane through its PH domain. Plasma membrane localization is a critical step in the activation of BTK. A fraction of BTK also shuttles between the nucleus and the cytoplasm, and nuclear export is mediated by the nuclear export receptor CRM1. .
- Cytosol
- Plasma membrane
- PubMed 11016936
- PubMed 25704810
- PubMed 10196179
- PubMed 10602036
- PubMed 19290921
- Tissue specificity (tau)
- 0.966665
- Expression inequality (Gini)
- 0.741323
Expression in transcripts per million
- Cells - EBV-transformed lymphocytes
- 114
- Spleen
- 49.73
- Whole Blood
- 28.49
- Lung
- 17.43
- Small Intestine - Terminal Ileum
- 9.89
Expression in transcripts per million
- Cells - EBV-transformed lymphocytes114
- Spleen49.73
- Whole Blood28.49
- Lung17.43
- Small Intestine - Terminal Ileum9.89
- Adipose - Subcutaneous6.07
- Nerve - Tibial4.94
- Brain - Spinal cord (cervical c-1)4.68
- Adipose - Visceral (Omentum)4.67
- Artery - Coronary4.08
- Bladder3.94
- Colon - Transverse3.66
- Esophagus - Muscularis3.19
- Artery - Aorta3.13
- Esophagus - Gastroesophageal Junction3.08
- Breast - Mammary Tissue2.95
- Minor Salivary Gland2.93
- Skin - Sun Exposed (Lower leg)2.85
- Prostate2.56
- Cervix - Endocervix2.55
- Skin - Not Sun Exposed (Suprapubic)2.53
- Colon - Sigmoid2.42
- Uterus2.38
- Vagina2.33
- Stomach2.32
And 29 more, listed on the interactive page.
- GO:0002250
- GO:0002721
- GO:0002755
- GO:0002902
- GO:0007498
- GO:0018108
- GO:0019722
- GO:0035556
- GO:0038095
- GO:0042113
- GO:0043123
- GO:0045087
- GO:0045579
- GO:0050853
- GO:0097190
- GO:0141111
- GO:1900227
- GO:0005634
- GO:0005737
- GO:0005829
- GO:0005886
- GO:0045121
- GO:0004713
- GO:0004715
- GO:0005515
- GO:0005524
- GO:0005547
- GO:0016004
- GO:0042802
- GO:0043274
regulation of catalytic activity
Studies
- biochemical: NVS_ENZ_hBTK, is one of one assay component(s) measured or calculated from the NVS_ENZ_hBTK assay. It is designed to make measurements of enzyme activity, a form of enzyme reporter, as detected with fluorescence intensity signals by Fluorescence and electrophoretic mobility shift technology.
Biological samples
- cell-free
Evidence source
Related records
Trials (1,490)
- 19(T2)28z1xx Chimeric Antigen Receptor (CAR) T Cells in People With B-Cell Cancers
- A 104-Week Study of Ritlecitinib Oral Capsules in Adults With Nonsegmental Vitiligo (Active and Stable) Tranquillo 2
- A 16-Week Study to Learn About the Study Medicine Called Ritlecitinib in Adults With Long Lasting Painful Red Skin Lumps, Known by the Medical Term, Hidradenitis Suppurativa, or HS.
- A 2×2 Factorial Randomized Controlled Trial for ERCP
- A 5-treatment, Study in Healthy Volunteers to Assess The Safety, Tolerability, and Pharmacokinetics of Four Controlled Release (CR) Pregabalin Tablet Formulations and the Immediate Release (IR) Formulation Administered Fasted
- A 52-week Study of Rilzabrutinib Efficacy and Safety Compared to Placebo in Adults Diagnosed With IgG4-related Disease
- A 52-Week Study of Ritlecitinib Oral Capsules in Adults and Adolescents With Nonsegmental Vitiligo (Active and Stable) Tranquillo
- A 52-Week Study to Learn About the Safety and Effects of Ritlecitinib in Participants With Nonsegmental Vitiligo
- A Bioavailability Study of SHR1459 on Healthy Chinese Volunteers
- A Clinical Study Evaluating the Safety and Efficacy of ZRMT Regimen in the Treatment of PCNSL
- A Clinical Study of iNSC Intervent Cerebral Hemorrhagic Stroke
- A Clinical Study on the Efficacy and Safety of Methotrexate (MTX) or Thiotepa (for MTX Intolerance) or Temozolomide (TMZ) Combined With Orelabrutinib and Selinexor in Relapsed/Refractory Primary or Secondary Central Nervous System Lymphoma(SELINA)
- A Clinical Study on the Treatment of LACC With Cadonilimab Combined With Chemotherapy Followed by CCRT
- A Clinical Trial of Buparlisib and Ibrutinib in Lymphoma
- A Clinical Trial of the Orelabrutinib in the Management of Refractory ITP
- A Combination of Acalabrutinib With R-CHOP for Patient Diffuse Large B-cell Lymphoma (DLBCL)
- A Combination of Acalabrutinib With R-CHOP in Subjects With Previously Untreated Non-GCB DLBCL (ACE-LY-312)
- A Combination Study of CAR-T Therapy in r/r B-NHL
- A Comparative Bioavailability and Pharmacokinetic Study of TNX-102 2.4 mg and Cyclobenzaprine 5 mg Tablets in Healthy Adults.
- A Comparison Between Propofol and Etomidate in Hysteroscopy on Effect of Postoperative Sedation and Cognitive Function in Elderly Patients
Drugs (24)
- Abivertinib Tyrosine-protein kinase BTK inhibitor
- Abivertinib maleate Tyrosine-protein kinase BTK inhibitor
- Acalabrutinib Tyrosine-protein kinase BTK inhibitor
- Acalabrutinib maleate Tyrosine-protein kinase BTK inhibitor
- BMS-986142 Tyrosine-protein kinase BTK inhibitor
- Branebrutinib Tyrosine-protein kinase BTK inhibitor
- Edralbrutinib Tyrosine-protein kinase BTK inhibitor
- Elsubrutinib Tyrosine-protein kinase BTK inhibitor
- Evobrutinib Tyrosine-protein kinase BTK inhibitor
- Fenebrutinib Tyrosine-protein kinase BTK inhibitor
- Ibrutinib Tyrosine-protein kinase BTK inhibitor
- MSC-2364447 Tyrosine-protein kinase BTK inhibitor
- Orelabrutinib Tyrosine-protein kinase BTK inhibitor
- Pirtobrutinib Tyrosine-protein kinase BTK inhibitor
- Poseltinib Tyrosine-protein kinase BTK inhibitor
- Rilzabrutinib Tyrosine-protein kinase BTK inhibitor
- Ritlecitinib TEC family kinase inhibitor
- Ritlecitinib tosylate TEC family kinase inhibitor
- Spebrutinib Tyrosine-protein kinase BTK inhibitor
- Spebrutinib besylate Tyrosine-protein kinase BTK inhibitor