TIRAP
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2Y92, 3UB2, 3UB3, 3UB4, 4FZ5, 4LQD
Identifiers
Aliases	TIRAP, BACTS1, Mal, MyD88-2, wyatt, toll-interleukin 1 receptor (TIR) domain containing adaptor protein, TIR domain containing adaptor protein
External IDs	OMIM: 606252 MGI: 2152213 HomoloGene: 14285 GeneCards: TIRAP
Gene location (Human) Chr. Chromosome 11 (human)[1] Band 11q24.2 Start 126,283,065 bp[1] End 126,298,845 bp[1]
Gene location (Mouse) Chr. Chromosome 9 (mouse)[2] Band 9|9 A4 Start 35,095,847 bp[2] End 35,111,587 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in monocyte bone marrow cells islet of Langerhans rectum smooth muscle tissue right lobe of liver minor salivary gland stromal cell of endometrium gallbladder appendix Top expressed in triceps brachii muscle vastus lateralis muscle conjunctival fornix sternocleidomastoid muscle primitive streak temporal muscle knee joint parotid gland cumulus cell otic placode More reference expression data BioGPS n/a
Gene ontology Molecular function protein-macromolecule adaptor activity protein homodimerization activity Toll-like receptor 2 binding Toll-like receptor 4 binding protein binding protein heterodimerization activity phosphatidylinositol-4,5-bisphosphate binding protein kinase C binding identical protein binding Cellular component cytoplasm cytosol membrane plasma membrane endocytic vesicle ruffle membrane Biological process myeloid cell differentiation regulation of innate immune response cellular response to bacterial lipopeptide positive regulation of toll-like receptor 3 signaling pathway positive regulation of interleukin-12 production positive regulation of chemokine (C-X-C motif) ligand 1 production positive regulation of chemokine (C-X-C motif) ligand 2 production immune system process positive regulation of JNK cascade MyD88-dependent toll-like receptor signaling pathway positive regulation of interleukin-15 production positive regulation of protein homodimerization activity cell surface receptor signaling pathway response to lipopolysaccharide TIRAP-dependent toll-like receptor 4 signaling pathway cellular response to lipoteichoic acid positive regulation of B cell proliferation regulation of interferon-beta production positive regulation of NF-kappaB transcription factor activity positive regulation of interleukin-8 production positive regulation of ERK1 and ERK2 cascade positive regulation of neutrophil chemotaxis positive regulation of tumor necrosis factor production positive regulation of toll-like receptor 4 signaling pathway positive regulation of I-kappaB kinase/NF-kappaB signaling positive regulation of toll-like receptor 2 signaling pathway 3'-UTR-mediated mRNA stabilization inflammatory response signal transduction defense response to Gram-positive bacterium innate immune response activation of NF-kappaB-inducing kinase activity Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 114609 117149 Ensembl ENSG00000150455 ENSMUSG00000032041 UniProt P58753 Q99JY1 RefSeq (mRNA) NM_001039661 NM_052887 NM_148910 NM_001318776 NM_001318777 NM_001177845 NM_001177846 NM_001177847 NM_054096 RefSeq (protein) NP_001034750 NP_001305705 NP_001305706 NP_683708 NP_001171316 NP_001171317 NP_001171318 NP_473437 Location (UCSC) Chr 11: 126.28 – 126.3 Mb Chr 9: 35.1 – 35.11 Mb PubMed search [3] [4]
Wikidata
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TIRAP (TIR domain containing adaptor protein) is an adapter molecule associated with toll-like receptors. The innate immune system recognizes microbial pathogens through Toll-like receptors (TLRs), which identify pathogen-associated molecular patterns. Different TLRs recognize different pathogen-associated molecular patterns and all TLRs have a Toll-interleukin 1 receptor (TIR) domain, which is responsible for signal transduction. The protein encoded by this gene is a TIR adaptor protein involved in the TLR4 signaling pathway of the immune system. It activates NF-kappa-B, MAPK1, MAPK3 and JNK, which then results in cytokine secretion and the inflammatory response. Alternative splicing of this gene results in several transcript variants; however, not all variants have been fully described.