Ignet
Search (e.g., vaccine, IFNG): Help
About
Home
Introduction
Statistics
Programs
Dignet
Gene
GenePair
BioSummarAI
Help & Docs
Documents
Help
FAQs
Links
Acknowledge
Disclaimer
Contact Us
UM Logo

UMMS Logo

UMMS Logo

Gene Information

Gene symbol: RIPK3

Gene name: receptor-interacting serine-threonine kinase 3

HGNC ID: 10021

Synonyms: RIP3

Related Genes

# Gene Symbol Number of hits
1 CRTC2 1 hits
2 GSTCD 1 hits
3 HNF4A 1 hits
4 MAPKAP1 1 hits
5 ZNHIT3 1 hits

Related Sentences

# PMID Sentence
1 11916906 Mutations of the hepatocyte nuclear factor-4alpha (HNF-4alpha) gene are associated with a subtype of maturity-onset diabetes of the young (MODY1) that is characterized by impaired insulin secretion in response to a glucose load.
2 11916906 In the present study, we showed, using a yeast two-hybrid screening assay, that thyroid hormone receptor interacting protein 3 (Trip3) interacted with HNF-4alpha, and their interaction was confirmed by the glutathione S-transferase pull-down assay.
3 11916906 Cotransfection experiments indicated that Trip3 could enhance (two- to threefold) the transcription activity of HNF-4alpha in COS-7 cells and MIN6 cells.
4 11916906 These results suggest that Trip3 is a coactivator of HNF-4alpha.
5 11916906 Mutation screening revealed that variation of the Trip3 gene is not a common cause of MODY/early-onset type 2 diabetes in Japanese individuals.
6 11916906 Trip3 may play an important role in glucose metabolism by regulating the transcription activity of HNF-4alpha.
7 17656577 The zinc finger HIT domain is a sequence motif found in many proteins, including thyroid hormone receptor interacting protein 3 (TRIP-3), which is possibly involved in maturity-onset diabetes of the young (MODY).
8 22266904 TOR complex 2 (TORC2) in Dictyostelium suppresses phagocytic nutrient capture independently of TORC1-mediated nutrient sensing.
9 22266904 The TOR protein kinase functions in two distinct complexes, TOR complex 1 (TORC1) and 2 (TORC2).
10 22266904 TORC1 is required for growth in response to growth factors, nutrients and the cellular energy state; TORC2 regulates AKT signaling, which can modulate cytoskeletal polarization.
11 22266904 However, loss of Dictyostelium TORC2 components Rictor/Pia, SIN1/RIP3 and Lst8 promotes nutrient particle uptake; inactivation of TORC2 leads to increased efficiency and speed of phagocytosis.
12 22266904 In contrast to phagocytosis, we show that macropinocytosis, an AKT-dependent process for cellular uptake of fluid phase nutrients, is not regulated by either of the TOR complexes.
13 22266904 The integrated and balanced regulation of TORC1 and TORC2 might be crucial in Dictyostelium to coordinate growth and energy needs with other essential TOR-regulated processes.