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Gene Information

Gene symbol: IKBKG

Gene name: inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma

HGNC ID: 5961

Synonyms: IKK-gamma, NEMO, Fip3p, FIP-3, FIP3, ZC2HC9

Related Genes

# Gene Symbol Number of hits
1 CYBB 1 hits
2 IFNGR1 1 hits
3 IFNGR2 1 hits
4 IKBKB 1 hits
5 IL10 1 hits
6 IL12B 1 hits
7 IL12RB1 1 hits
8 IRAK4 1 hits
9 IRF8 1 hits
10 ISG15 1 hits
11 NFKB1 1 hits
12 STAT1 1 hits

Related Sentences

# PMID Sentence
1 14763335 The aim of this review is to describe 3 new syndromes with a genetic predisposition of infectious diseases: IL-12-IFN gamma axis deficiency (Mendelian susceptibility to mycobacterial disease), STAT1 deficiency (predisposition to viral disease) and NEMO and IRAK-4 deficiencies (predisposition to infections caused by pyogenic bacteria).
2 14963119 Mice treated intranasally with interleukin-10 or with a specific cell-permeable peptide that blocks the association of the catalytic subunit IKKbeta with the regulatory protein NEMO showed a striking reduction of lung NF-kappaB DNA binding activity, chemokine gene expression, and airway inflammation in response to RSV infection.
3 16426002 Tumor necrosis factor (TNF) production in PBMC supernatants was measured by an enzyme-linked immunosorbent assay after TLR ligand stimulation and was dependent on gene transcription and NF-kappaB activation.
4 16426002 Finally, three patients with a mutation in the IKBKG gene, encoding the NF-kappaB essential modulator (NEMO) protein, were evaluated as disease controls and were almost uniformly below the standard deviation of healthy donors for all ligands tested.
5 16950813 IRAK4 and NEMO mutations in otherwise healthy children with recurrent invasive pneumococcal disease.
6 25453225 Since 1996, nine MSMD-causing genes, including seven autosomal (IFNGR1, IFNGR2, STAT1, IL12B, IL12RB1, ISG15, and IRF8) and two X-linked (NEMO, and CYBB) genes have been discovered.
7 25453225 These disorders impair the production of (IL12B, IL12RB1, IRF8, ISG15, NEMO) or the response to (IFNGR1, IFNGR2, STAT1, IRF8, CYBB) IFN-γ.
8 25453225 Since 1996, nine MSMD-causing genes, including seven autosomal (IFNGR1, IFNGR2, STAT1, IL12B, IL12RB1, ISG15, and IRF8) and two X-linked (NEMO, and CYBB) genes have been discovered.
9 25453225 These disorders impair the production of (IL12B, IL12RB1, IRF8, ISG15, NEMO) or the response to (IFNGR1, IFNGR2, STAT1, IRF8, CYBB) IFN-γ.