Fkbp1a gene
TīmeklisFKBP1A has 5,429 functional associations with biological entities spanning 8 categories (molecular profile, organism, functional term, phrase or reference, chemical, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 83 datasets. TīmeklisFKBP1A is part of cluster 28 Placenta - Pregnancy with confidence i Confidence is the fraction of times a gene was assigned to the cluster in repeated clustering, and …
Fkbp1a gene
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Tīmeklis2024. gada 21. marts · FKBP11 (FKBP Prolyl Isomerase 11) is a Protein Coding gene. Diseases associated with FKBP11 include Osteogenesis Imperfecta, Type V and Caffey Disease . Gene Ontology (GO) annotations related to this gene include peptidyl-prolyl cis-trans isomerase activity and FK506 binding . An important paralog of this gene is … TīmeklisFK506, a macrolide derived from Streptomyces inhibits peptidyl–prolyl isomerase activity by binding to the immunophilin FKBP1A (FK506-binding protein). The …
TīmeklisThe protein encoded by this gene is a member of the immunophilin protein family which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It interacts with several intracellular … Tīmeklis2024. gada 29. marts · FKBP prolyl isomerase 1A. Gene ID: 2280, updated on 29-Mar-2024. Gene type: protein coding. Also known as: FKBP1; PKC12; PKCI2; FKBP12; …
TīmeklisThe protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding … TīmeklisFKBP1A. General description of the gene and the encoded protein (s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas …
TīmeklisBecause systemic delivery of the Fkbp8 gene reduced the metastatic progression of two different highly aggressive mouse tumor cell types (Fig. 1 A and B), we then tested whether up-regulation of the human Fkbp1a gene, the best characterized member of the FKBP gene family, could produce similar anti-tumor progression effects in mice.
Peptidyl-prolyl cis-trans isomerase FKBP1A is an enzyme that in humans is encoded by the FKBP1A gene. It is also commonly referred to as FKBP-12 or FKBP12 and is a member of a family of FK506-binding proteins (FKBPs). mass shootings where guns were bought legallyTīmeklis2024. gada 10. janv. · UPK1A (Uroplakin 1A) is a Protein Coding gene. Diseases associated with UPK1A include Transitional Cell Carcinoma and Cystitis . Gene … hyer family servicesTīmeklis2024. gada 21. marts · FKBP1A (FKBP Prolyl Isomerase 1A) is a Protein Coding gene. Diseases associated with FKBP1A include Fibrodysplasia Ossificans Progressiva and Subependymal Glioma . Among its related pathways are TGF-beta receptor signaling … RYR2 (Ryanodine Receptor 2) is a Protein Coding gene. Diseases associated with … Gene fusions also decouple kinase activity from the cell membrane and render it … SOD1 (Superoxide Dismutase 1) is a Protein Coding gene. Diseases … RPS6KB1 (Ribosomal Protein S6 Kinase B1) is a Protein Coding gene. Diseases … RICTOR (RPTOR Independent Companion Of MTOR Complex 2) is a Protein … APP (Amyloid Beta Precursor Protein) is a Protein Coding gene. Diseases … TGFB1 (Transforming Growth Factor Beta 1) is a Protein Coding gene. Diseases … WT1 (WT1 Transcription Factor) is a Protein Coding gene. Diseases … hyeres triathlonTīmeklis2016. gada 14. sept. · FKBP1A (human) Gene Target - PubChem Apologies, we are having some trouble retrieving data from our servers... PUGVIEW FETCH ERROR: 403 Forbidden National Center for Biotechnology Information 8600 Rockville Pike, Bethesda, MD, 20894 USA Contact Policies FOIA HHS Vulnerability Disclosure National Library … hyeres t shirtTīmeklis2024. gada 21. marts · FKBP10 (FKBP Prolyl Isomerase 10) is a Protein Coding gene. Diseases associated with FKBP10 include Bruck Syndrome 1 and Osteogenesis Imperfecta, Type Xi . Among its related pathways are Type I collagen synthesis in the context of osteogenesis imperfecta . hyeres train stationTīmeklis2003. gada 25. nov. · FKBP gene expression coordinately induces the expression of the antiinvasive Sdc1 gene and suppresses the proinvasive MMP9 gene. Conversely, … hyer furnitureTīmeklis2024. gada 15. jūl. · Moreover, FKBP prolyl isomerase 1A (FKBP1A) was a target of miR-338-3p. This investigation demonstrated that SNHG15 may serve as a competing endogenous RNA (ceRNA) to regulate miR-338-3p and FKBP1A. Finally, the involvement of miR-338-3p and FKBP1A in SNHG15-mediated biological function … hyer hardware