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bn:03546929n
Noun Concept
Categories: Peripheral membrane proteins, Genes on human chromosome X, Tyrosine kinases, Articles with short description
EN
Bruton's tyrosine kinase  BTK  ATK  BPK  tyrosine-protein kinase BTK isoform
EN
Bruton's tyrosine kinase, also known as tyrosine-protein kinase BTK, is a tyrosine kinase that is encoded by the BTK gene in humans. Wikipedia
English:
gene
Definitions
Relations
Sources
EN
Bruton's tyrosine kinase, also known as tyrosine-protein kinase BTK, is a tyrosine kinase that is encoded by the BTK gene in humans. Wikipedia
A protein Wikipedia Disambiguation
Protein-coding gene in the species Homo sapiens Wikidata
A tyrosine-protein kinase that has a role in the development of B cells. Wiktionary
IS A
gene
protein
HAS PART
protein kinase domain
SH2 domain
SH3 domain
Btk-type zinc finger
pleckstrin homology domain
BIOLOGICAL PROCESS
apoptosis
protein phosphorylation
autophosphorylation
phosphorylation
innate immune response
CELL COMPONENT
cell membrane
nucleus
cytoplasm
cytosol
lipid raft
CHROMOSOME
X chromosome
ENCODED BY
Bruton's tyrosine kinase
ENCODES
Bruton's tyrosine kinase
FOUND IN TAXON
early modern human
GENETIC ASSOCIATION
X-linked agammaglobulinemia
MOLECULAR FUNCTION
plasma protein binding
PHYSICALLY INTERACTS WITH
ibrutinib
Wikipedia
EN
Bruton's tyrosine kinase
Wikidata
EN
Bruton's tyrosine kinase, BTK
Wiktionary
EN
Bruton's tyrosine kinase
Wikipedia Redirections
EN
Agmx1, AGMX1, BPK, Bruton's tyrosine kinase inhibitor, Bruton agammaglobulinemia tyrosine kinase, Bruton tyrosine kinase, BTK (gene), BTK inhibitor, Imd1, IMD1, Psctk1, PSCTK1
Wikidata Alias
EN
agammaglobulinaemia tyrosine kinase, Agammaglobulinemia tyrosine kinase, AGMX1, AT, ATK, B-cell progenitor kinase, BPK, Bruton's tyrosine kinase, Bruton agammaglobulinemia tyrosine kinase, Bruton tyrosine kinase, BTK, dominant-negative kinase-deficient Brutons tyrosine kinase, IGHD3, IMD1, PSCTK1, truncated Bruton agammaglobulinemia tyrosine kinase, tyrosine-protein kinase BTK, XLA, tyrosine-protein kinase BTK isoform (lacking exon 13 to 17)

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