Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1147
Gene name Gene Name - the full gene name approved by the HGNC.
Component of inhibitor of nuclear factor kappa B kinase complex
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CHUK
Synonyms (NCBI Gene) Gene synonyms aliases
BPS2, IKBKA, IKK-1, IKK-alpha, IKK1, IKKA, NFKBIKA, TCF16
Disease Acronyms (UniProt) Disease acronyms from UniProt database
BPS2
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q24.31
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the serine/threonine protein kinase family. The encoded protein, a component of a cytokine-activated protein complex that is an inhibitor of the essential transcription factor NF-kappa-B complex, phosphorylates sites that tri
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs267606736 G>A Pathogenic Coding sequence variant, stop gained, non coding transcript variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT005552 hsa-miR-15a-5p Luciferase reporter assay, qRT-PCR, Western blot 20711193
MIRT005552 hsa-miR-15a-5p Luciferase reporter assay, qRT-PCR, Western blot 20711193
MIRT005552 hsa-miR-15a-5p Luciferase reporter assay, qRT-PCR, Western blot 20711193
MIRT005552 hsa-miR-15a-5p Luciferase reporter assay, qRT-PCR, Western blot 20711193
MIRT005554 hsa-miR-16-5p Luciferase reporter assay, qRT-PCR, Western blot 20711193
Transcription factors
Transcription factor Regulation Reference
ETS1 Activation 15469934
TP53 Repression 15469934
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002223 Process Stimulatory C-type lectin receptor signaling pathway TAS
GO:0002479 Process Antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent TAS
GO:0002756 Process MyD88-independent toll-like receptor signaling pathway TAS
GO:0003009 Process Skeletal muscle contraction IEA
GO:0004672 Function Protein kinase activity IDA 20434986
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600664 1974 ENSG00000213341
Protein
UniProt ID O15111
Protein name Inhibitor of nuclear factor kappa-B kinase subunit alpha (I-kappa-B kinase alpha) (IKK-A) (IKK-alpha) (IkBKA) (IkappaB kinase) (EC 2.7.11.10) (Conserved helix-loop-helix ubiquitous kinase) (I-kappa-B kinase 1) (IKK-1) (IKK1) (Nuclear factor NF-kappa-B inh
Protein function Serine kinase that plays an essential role in the NF-kappa-B signaling pathway which is activated by multiple stimuli such as inflammatory cytokines, bacterial or viral products, DNA damages or other cellular stresses (PubMed:18626576, PubMed:92
PDB 3BRT , 5EBZ , 5TQW , 5TQX , 5TQY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 15 298 Protein kinase domain Domain
PF18397 IKBKB_SDD 386 659 IQBAL scaffold dimerization domain Domain
PF12179 IKKbetaNEMObind 707 743 I-kappa-kinase-beta NEMO binding domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed.
Sequence
Sequence length 745
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Antifolate resistance
MAPK signaling pathway
Ras signaling pathway
Chemokine signaling pathway
NF-kappa B signaling pathway
FoxO signaling pathway
mTOR signaling pathway
PI3K-Akt signaling pathway
Apoptosis
Osteoclast differentiation
Toll-like receptor signaling pathway
NOD-like receptor signaling pathway
RIG-I-like receptor signaling pathway
Cytosolic DNA-sensing pathway
C-type lectin receptor signaling pathway
IL-17 signaling pathway
Th1 and Th2 cell differentiation
Th17 cell differentiation
T cell receptor signaling pathway
B cell receptor signaling pathway
TNF signaling pathway
Adipocytokine signaling pathway
Alcoholic liver disease
Alzheimer disease
Epithelial cell signaling in Helicobacter pylori infection
Pathogenic Escherichia coli infection
Shigellosis
Salmonella infection
Yersinia infection
Chagas disease
Toxoplasmosis
Hepatitis C
Hepatitis B
Measles
Human cytomegalovirus infection
Influenza A
Human papillomavirus infection
Human T-cell leukemia virus 1 infection
Kaposi sarcoma-associated herpesvirus infection
Herpes simplex virus 1 infection
Epstein-Barr virus infection
Human immunodeficiency virus 1 infection
Coronavirus disease - COVID-19
Pathways in cancer
Chemical carcinogenesis - reactive oxygen species
Pancreatic cancer
Prostate cancer
Chronic myeloid leukemia
Acute myeloid leukemia
Small cell lung cancer
PD-L1 expression and PD-1 checkpoint pathway in cancer
Lipid and atherosclerosis
Fluid shear stress and atherosclerosis
  Activation of NF-kappaB in B cells
ER-Phagosome pathway
NOD1/2 Signaling Pathway
TICAM1, RIP1-mediated IKK complex recruitment
RIP-mediated NFkB activation via ZBP1
AKT phosphorylates targets in the cytosol
Downstream TCR signaling
FCERI mediated NF-kB activation
TAK1 activates NFkB by phosphorylation and activation of IKKs complex
Regulation of TNFR1 signaling
TNFR1-induced NFkappaB signaling pathway
IKBKB deficiency causes SCID
IKBKG deficiency causes anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) (via TLR)
IkBA variant leads to EDA-ID
Dectin-1 mediated noncanonical NF-kB signaling
CLEC7A (Dectin-1) signaling
Constitutive Signaling by AKT1 E17K in Cancer
NIK-->noncanonical NF-kB signaling
MAP3K8 (TPL2)-dependent MAPK1/3 activation
Interleukin-1 signaling
TRAF6 mediated NF-kB activation
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10
IRAK1 recruits IKK complex
IKK complex recruitment mediated by RIP1
IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cocoon syndrome COCOON SYNDROME rs267606736 20961246
Diabetes mellitus Diabetes Mellitus, Non-Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
30054458
Microcephaly Microcephaly rs397704721, rs267607176, rs267607177, rs397704725, rs267606717, rs267606718, rs199422202, rs121434311, rs199422203, rs199422126, rs387906274, rs121434305, rs199422125, rs199422135, rs189678019
View all (280 more)
Multiple congenital anomalies Multiple congenital anomalies rs1057517732 20961246
Unknown
Disease term Disease name Evidence References Source
Bartsocas-Papas Syndrome Bartsocas-Papas syndrome 2 GenCC
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Agammaglobulinemia Associate 39812688
Breast Neoplasms Associate 15808510, 21575199, 23178494, 25377085, 28006839, 40650045
Carcinoma Hepatocellular Associate 19331697, 27409165, 32265434
Carcinoma Ovarian Epithelial Associate 27537390
Carcinoma Renal Cell Associate 37847185
Carcinoma Squamous Cell Associate 21170261
Cholangiocarcinoma Associate 29620225
Colorectal Neoplasms Associate 12771929, 19513071, 35173303
Crohn Disease Associate 26215868, 34629811
Cystic Fibrosis Associate 10706733, 12507912, 12762338