WebPromotes the cell surface stability of iRhom1/RHBDF1 and iRhom2/RHBDF2 and prevents their degradation via the endolysosomal pathway. By acting on iRhoms, involved in ADAM17-mediated shedding of TNF, amphiregulin/AREG, HBEGF and TGFA from the cell surface (PubMed:29897333, PubMed:29897336). WebMar 9, 2024 · iRHOM2 is a proteolytically inactive member of the seven transmembrane family of Rhomboid serine proteases 6. iRHOM2 can control activation and trafficking of ADAM17 (also known as TACE; TNFα...
TOC Cancer Genetics Web
WebRHBDF2 Gene, Drug Resistance, Tissue Distribution, Mutation Distribution, Variants, RHBDF2 Genome Browser, RHBDF2 References ... Mouse insertional mutagenesis experiments support the designation of RHBDF2 as a cancer causing gene. More information. ... TOC, TOCG, iRhom2, CCDS32743.1, Q6PJF5, ENSG00000129667.12 more. NM_024599.5, … WebDec 22, 2024 · Two iRHOM proteins, iRHOM1 and iRHOM2, are encoded in metazoans by the RHBDF1 and RHBDF2 genes, respectively. iRHOM1 is expressed in most tissues, but not … how to remove cross threaded lug nut
Human iRHOM2/RHBDF2 Antibody (MAB10048) Bio-Techne
WebJul 1, 2008 · Inactive rhomboid protein 2 Short names iRhom2 Alternative names Rhomboid 5 homolog 2 Rhomboid family member 2 Rhomboid veinlet-like protein 5 Rhomboid veinlet-like protein 6 Gene names Name RHBDF2 Synonyms IRHOM2, RHBDL5, RHBDL6 Organism names Organism Homo sapiens (Human) Taxonomic identifier 9606 NCBI Taxonomic … WebApr 1, 2024 · iRhom2: Esophageal cancer and inflammatory disease. RHBDF2 is the only known highly penetrant genetic predisposition to OSCC, although how and why … WebJul 4, 2024 · Tylosis with esophageal cancer syndrome (TOC) is a rare autosomal dominant proliferative skin disease caused by missense mutations in the rhomboid 5 homolog 2 (RHBDF2) gene. TOC is characterized by thickening of the skin in the palms and feet and is strongly linked with the development of esophageal squamous cell carcinoma. how to remove crown from quartz watch