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    RASGRP2 RAS guanyl releasing protein 2 [ Homo sapiens (human) ]

    Gene ID: 10235, updated on 10-Oct-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    [Study on the Role of RASGRP2 in Vascular Endothelial Cells].


    11/7/2023
    RASGRP2 is a potential immune-related biomarker and regulates mitochondrial-dependent apoptosis in lung adenocarcinoma.


    03/1/2023
    Novel RASGRP2 variants in platelet function defects: Indian study.


    05/7/2022
    CalDAG-GEFI Deficiency in a Family with Symptomatic Heterozygous and Homozygous Carriers of a Likely Pathogenic Variant in RASGRP2.


    02/5/2022
    The Role of RASGRP2 in Vascular Endothelial Cells-A Mini Review.


    01/22/2022
    RasGRP2 inhibits glyceraldehyde-derived toxic advanced glycation end-products from inducing permeability in vascular endothelial cells.


    11/13/2021
    Mutations in RASGRP2 gene identified in patients misdiagnosed as Glanzmann thrombasthenia patients.


    10/16/2021
    A novel missense variant in the RASGRP2 gene in patients with moderate to severe bleeding disorder.


    02/13/2021
    RasGRP2 Structure, Function and Genetic Variants in Platelet Pathophysiology.


    11/21/2020
    RASGRP2 mutation is associated with bleeding disorders.


    04/25/2020
    RASGRP2 was identified to be involved in the pathogenesis of rheumatoid arthritis by promoting adhesion, migration and IL-6 production from fibroblast-like synoviocytes


    08/24/2019
    results indicate that CD38 promotes RasGRP2/Rap1-mediated CLL cell adhesion and migration by increasing intracellular Ca2+ levels.


    04/13/2019
    we here describe a novel mutation in RASGRP2 that affects both expression and function of CalDAG-GEFI and that causes impaired platelet adhesive function and significant bleeding in humans.


    08/11/2018
    Eleven cases with unexplained bleeding or platelet disorders harbored 11 different, previously unreported RASGRP2 variants that were biallelic and likely pathogenic.


    09/30/2017
    These patients are the first cases of a CalDAG-GEFI deficiency due to homozygous RASGRP2 mutations that are linked to defects in both leukocyte and platelet integrin activation.


    08/5/2017
    These studies identify RasGRP2 as a novel substrate of ERK1/2 and define a negative-feedback loop that regulates the BRaf-MEK-ERK signaling cascade. This negative-feedback loop determines the amplitude and duration of active ERK1/2.


    05/13/2017
    RasGRP2 is exceptional in that its C1 domain has very weak binding affinity (Kd = 2890 +/- 240 nm for [(3)H]phorbol 12,13-dibutyrate. We have identified four amino acid residues responsible for this lack of sensitivity. Replacing Asn(7), Ser(8), Ala(19), and Ile(21) with the corresponding residues from RasGRP1/3 (Thr(7), Tyr(8), Gly(19), and Leu(21), respectively) conferred potent binding affinity (Kd = 1.47 +/- 0.03 nm).


    12/17/2016
    Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleeding.


    09/6/2014
    phosphorylation of CalDAG-GEFI is a critical mechanism by which PKA controls Rap1b-dependent platelet aggregation


    03/22/2014
    RasGRP2 increases cell viability and cell-matrix adhesion through increased Ras expression and Rap1 activation, respectively, in endothelial cells.


    02/8/2014
    NIH3T3 cells were found nonpermissive to mtHSV but they became permissive following transformation with the Rasgrp2 gene. This effect was linked to the activation of the Ras-PKR signaling pathway.


    02/1/2014
    analyzed the 5'-flanking region of rasgrp2 gene by a luciferase assay, which revealed that not only a promoter but also silencer regions were present upstream of D1E, suggesting rasgrp2 expression is controlled by a combination of promotion and repression


    11/27/2010
    CalDAG-GEFI plays a role in inside-out signaling to alphaIIbbeta3


    01/21/2010
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