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    FAM83D family with sequence similarity 83 member D [ Homo sapiens (human) ]

    Gene ID: 81610, updated on 10-Dec-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    FAM83D promotes the progression of 4NQO-induced esophageal carcinoma via inhibiting FBWX7.

    FAM83D promotes the progression of 4NQO-induced esophageal carcinoma via inhibiting FBWX7.
    Li J, Tian J, Ma M, Qin Z, Cao B, Yang J, Wang X, Yang X.

    11/6/2024
    METTL3 regulates FAM83D m[6]A modification to accelerate tumorigenesis of triple-negative breast cancer via the Wnt/beta-catenin pathway.

    METTL3 regulates FAM83D m(6)A modification to accelerate tumorigenesis of triple-negative breast cancer via the Wnt/β-catenin pathway.
    Yu X, Li Y, Kong F, Xu Q.

    01/16/2024
    Systematic analysis of the oncogenic role of FAM83D across cancers based on data mining.

    Systematic analysis of the oncogenic role of FAM83D across cancers based on data mining.
    Geng Y, Liu J, Wang Z, Liu T, Peng X, Huang Y., Free PMC Article

    03/29/2023
    miRNA-142-3p functions as a potential tumor suppressor directly targeting FAM83D in the development of ovarian cancer.

    miRNA-142-3p functions as a potential tumor suppressor directly targeting FAM83D in the development of ovarian cancer.
    Gao G, Guo X, Gu W, Lu Y, Chen Z., Free PMC Article

    05/14/2022
    Immune implication of FAM83D gene in hepatocellular carcinoma.

    Immune implication of FAM83D gene in hepatocellular carcinoma.
    Meng T, Tong Z, Yang MY, Zhang Y, Liu Y, Wang ZZ, Zhu LX, Wu J., Free PMC Article

    12/18/2021
    Fam83d modulates MAP kinase and AKT signaling and is induced during neurogenic skeletal muscle atrophy.

    Fam83d modulates MAP kinase and AKT signaling and is induced during neurogenic skeletal muscle atrophy.
    Cooper LM, Hanson A, Kavanagh JA, Waddell DS.

    08/14/2021
    FAM83D promotes epithelial-mesenchymal transition, invasion and cisplatin resistance through regulating the AKT/mTOR pathway in non-small-cell lung cancer.

    FAM83D promotes epithelial-mesenchymal transition, invasion and cisplatin resistance through regulating the AKT/mTOR pathway in non-small-cell lung cancer.
    Yin C, Lin X, Wang Y, Liu X, Xiao Y, Liu J, Snijders AM, Wei G, Mao JH, Zhang P.

    01/2/2021
    circFOXM1 promotes proliferation of non-small cell lung carcinoma cells by acting as a ceRNA to upregulate FAM83D.

    circFOXM1 promotes proliferation of non-small cell lung carcinoma cells by acting as a ceRNA to upregulate FAM83D.
    Yu C, Cheng Z, Cui S, Mao X, Li B, Fu Y, Wang H, Jin H, Ye Q, Zhao X, Jiang L, Qin W., Free PMC Article

    12/12/2020
    FAM83D promotes ovarian cancer progression and its potential application in diagnosis of invasive ovarian cancer.

    FAM83D promotes ovarian cancer progression and its potential application in diagnosis of invasive ovarian cancer.
    Zhang Q, Yu S, Lok SIS, Wong AST, Jiao Y, Lee LTO., Free PMC Article

    08/13/2020
    Overexpressed in tumors, family with sequence similarity 83 member D protein FAM83D (FAM83D) is associated with gender, AJCC stage, tumor recurrence and survival in hepatocellular carcinoma (HCC).

    FAM83D is associated with gender, AJCC stage, overall survival and disease-free survival in hepatocellular carcinoma.
    Liu X, Gao H, Zhang J, Xue D., Free PMC Article

    07/11/2020
    FAM83D promotes HCC recurrence by promoting CD44 expression and CD44+ CSCs malignancy.

    FAM83D associates with high tumor recurrence after liver transplantation involving expansion of CD44+ carcinoma stem cells.
    Lin B, Chen T, Zhang Q, Lu X, Zheng Z, Ding J, Liu J, Yang Z, Geng L, Wu L, Zhou L, Zheng S., Free PMC Article

    03/3/2018
    FAM83D knockdown up-regulated the protein expression level of F-box and WD repeat domain-containing 7 (FBXW7), but diminished the Notch1 protein expression level.

    FAM83D knockdown regulates proliferation, migration and invasion of colorectal cancer through inhibiting FBXW7/Notch-1 signalling pathway.
    Mu Y, Zou H, Chen B, Fan Y, Luo S.

    02/24/2018
    Higher level of FAM83D expression is positively correlated with an increase in genome instability in many cancer.

    Prognostic significance of FAM83D gene expression across human cancer types.
    Walian PJ, Hang B, Mao JH., Free PMC Article

    12/17/2016
    upregulation of FAM83D, a potential oncotarget gene, may be triggered by epigenetic events and can contribute to hepatocarcinogenesis

    Upregulation of FAM83D affects the proliferation and invasion of hepatocellular carcinoma.
    Liao W, Liu W, Liu X, Yuan Q, Ou Y, Qi Y, Huang W, Wang Y, Huang J., Free PMC Article

    08/13/2016
    NMR-derived secondary chemical shifts and relaxation properties show that the Chica LC8 binding domain is essentially disordered with a dynamically restricted segment in one linker between motifs.

    The Anchored Flexibility Model in LC8 Motif Recognition: Insights from the Chica Complex.
    Clark S, Nyarko A, Löhr F, Karplus PA, Barbar E., Free PMC Article

    05/14/2016
    Taken together, these results demonstrate that FAM83D is a novel oncogene in HCC development and may constitute a potential therapeutic target in HCC.

    FAM83D activates the MEK/ERK signaling pathway and promotes cell proliferation in hepatocellular carcinoma.
    Wang D, Han S, Peng R, Wang X, Yang XX, Yang RJ, Jiao CY, Ding D, Ji GW, Li XC.

    05/2/2015
    Results demonstrate that FAM83D has prognostic value for breast cancer patients and is a novel oncogene in breast cancer development that at least in part acts through mTOR hyper-activation by inhibiting FBXW7.

    FAM83D promotes cell proliferation and motility by downregulating tumor suppressor gene FBXW7.
    Wang Z, Liu Y, Zhang P, Zhang W, Wang W, Curr K, Wei G, Mao JH., Free PMC Article

    11/22/2014
    interaction partner of the chromokinesin Kid that is required for the generation of polar ejection forces and chromosome congression

    The spindle protein CHICA mediates localization of the chromokinesin Kid to the mitotic spindle.
    Santamaria A, Nagel S, Sillje HHW, Nigg EA.

    01/21/2010
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