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Ask your administrator if you think this is wrong. ======= NFKB2 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: NFKB2 * **<color #00a2e8>Official Name</color>**: nuclear factor kappa B subunit 2 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=4791|4791]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q00653|Q00653]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=NFKB2&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20NFKB2|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/164012|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: This gene encodes a subunit of the transcription factor complex nuclear factor-kappa-B (NFkB). The NFkB complex is expressed in numerous cell types and functions as a central activator of genes involved in inflammation and immune function. The protein encoded by this gene can function as both a transcriptional activator or repressor depending on its dimerization partner. The p100 full-length protein is co-translationally processed into a p52 active form. Chromosomal rearrangements and translocations of this locus have been observed in B cell lymphomas, some of which may result in the formation of fusion proteins. There is a pseudogene for this gene on chromosome 18. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]. * **<color #00a2e8>UniProt Summary</color>**: NF-kappa-B is a pleiotropic transcription factor present in almost all cell types and is the endpoint of a series of signal transduction events that are initiated by a vast array of stimuli related to many biological processes such as inflammation, immunity, differentiation, cell growth, tumorigenesis and apoptosis. NF-kappa-B is a homo- or heterodimeric complex formed by the Rel-like domain-containing proteins RELA/p65, RELB, NFKB1/p105, NFKB1/p50, REL and NFKB2/p52. The dimers bind at kappa-B sites in the DNA of their target genes and the individual dimers have distinct preferences for different kappa-B sites that they can bind with distinguishable affinity and specificity. Different dimer combinations act as transcriptional activators or repressors, respectively. NF-kappa-B is controlled by various mechanisms of post-translational modification and subcellular compartmentalization as well as by interactions with other cofactors or corepressors. NF-kappa-B complexes are held in the cytoplasm in an inactive state complexed with members of the NF- kappa-B inhibitor (I-kappa-B) family. In a conventional activation pathway, I-kappa-B is phosphorylated by I-kappa-B kinases (IKKs) in response to different activators, subsequently degraded thus liberating the active NF-kappa-B complex which translocates to the nucleus. In a non-canonical activation pathway, the MAP3K14- activated CHUK/IKKA homodimer phosphorylates NFKB2/p100 associated with RelB, inducing its proteolytic processing to NFKB2/p52 and the formation of NF-kappa-B RelB-p52 complexes. The NF-kappa-B heterodimeric RelB-p52 complex is a transcriptional activator. The NF-kappa-B p52-p52 homodimer is a transcriptional repressor. NFKB2 appears to have dual functions such as cytoplasmic retention of attached NF-kappa-B proteins by p100 and generation of p52 by a cotranslational processing. The proteasome-mediated process ensures the production of both p52 and p100 and preserves their independent function. p52 binds to the kappa-B consensus sequence 5'-GGRNNYYCC-3', located in the enhancer region of genes involved in immune response and acute phase reactions. p52 and p100 are respectively the minor and major form; the processing of p100 being relatively poor. Isoform p49 is a subunit of the NF-kappa-B protein complex, which stimulates the HIV enhancer in synergy with p65. In concert with RELB, regulates the circadian clock by repressing the transcriptional activator activity of the CLOCK- ARNTL/BMAL1 heterodimer. {ECO:0000269|PubMed:7925301}. <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'> |Death| |Ank 2| |Ank| |RHD| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |Bcl3/NF-kappaB2 complex| |follicular dendritic cell differentiation| |follicular dendritic cell activation| |germinal center formation| |spleen development| |positive regulation of type I interferon production| |NIK/NF-kappaB signaling| |regulation of type I interferon production| |positive regulation of NF-kappaB transcription factor activity| |positive regulation of DNA-binding transcription factor activity| |rhythmic process| |aging| |adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains| |transcription coactivator activity| |response to lipopolysaccharide| |response to molecule of bacterial origin| |extracellular matrix organization| |extracellular structure organization| |regulation of DNA-binding transcription factor activity| |DNA-binding transcription activator activity, RNA polymerase II-specific| |positive regulation of cytokine production| |RNA polymerase II proximal promoter sequence-specific DNA binding| |hematopoietic or lymphoid organ development| |adaptive immune response| |immune system development| |DNA-binding transcription factor activity| |response to bacterium| |regulation of cytokine production| |response to lipid| |anatomical structure formation involved in morphogenesis| |cell activation| |response to cytokine| |positive regulation of transcription by RNA polymerase II| |response to other organism| |response to external biotic stimulus| |response to biotic stimulus| |positive regulation of transcription, DNA-templated| |response to oxygen-containing compound| |DNA-binding transcription factor activity, RNA polymerase II-specific| |positive regulation of nucleic acid-templated transcription| |positive regulation of RNA biosynthetic process| |intracellular signal transduction| |positive regulation of RNA metabolic process| |positive regulation of multicellular organismal process| |positive regulation of molecular function| |immune response| |positive regulation of nucleobase-containing compound metabolic process| |positive regulation of macromolecule biosynthetic process| |positive regulation of cellular biosynthetic process| |positive regulation of gene expression| |positive regulation of biosynthetic process| </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:exp17|DABN 20μM R00 exp17]]|-2.35| |[[:results:exp46|HMS-I1 1μM R01 exp46]]|-2.05| |[[:results:exp116|AICAR 240μM R03 exp116]]|-1.81| |[[:results:exp212|Phenformin 20μM R05 exp212]]|-1.78| |[[:results:exp7|Bortezomib 0.05μM R00 exp7]]|-1.74| |[[:results:exp508|NN-Dimethylsphingosine 2.5μM R08 exp508]]|-1.73| |[[:results:exp279|D-Fructose 10000μM R06 exp279]]|2.26| </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: 6/739 ^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|2/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|3/15| |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>**: 4130 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 4.48 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='NFKB2 Expression in NALM6 Cells: 4.48'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:36by 127.0.0.1