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    GTF2I general transcription factor IIi [ Homo sapiens (human) ]

    Gene ID: 2969, updated on 27-Nov-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    ChIP-seq analysis found IL21R, a target gene of GTF2I-the susceptibility gene for primary biliary cholangitis in Chinese Han.

    ChIP-seq analysis found IL21R, a target gene of GTF2I-the susceptibility gene for primary biliary cholangitis in Chinese Han.
    Wu Z, Li H, Xu H, Feng F, Zhang F, Zhang S, Wang L, Li Y.

    04/17/2024
    Loss of GTF2I promotes neuronal apoptosis and synaptic reduction in human cellular models of neurodevelopment.

    Loss of GTF2I promotes neuronal apoptosis and synaptic reduction in human cellular models of neurodevelopment.
    Adams JW, Vinokur A, de Souza JS, Austria C, Guerra BS, Herai RH, Wahlin KJ, Muotri AR., Free PMC Article

    04/2/2024
    GTF2I mutation in micronodular thymoma with lymphoid stroma.

    GTF2I mutation in micronodular thymoma with lymphoid stroma.
    Bille A, Fryer K, Wallace A, Nonaka D.

    01/26/2024
    Neuronal Gtf2i deletion alters mitochondrial and autophagic properties.

    Neuronal Gtf2i deletion alters mitochondrial and autophagic properties.
    Nir Sade A, Levy G, Schokoroy Trangle S, Elad Sfadia G, Bar E, Ophir O, Fischer I, Rokach M, Atzmon A, Parnas H, Rosenberg T, Marco A, Elroy Stein O, Barak B., Free PMC Article

    12/20/2023
    DUX4-r exerts a neomorphic activity that depends on GTF2I in acute lymphoblastic leukemia.

    DUX4-r exerts a neomorphic activity that depends on GTF2I in acute lymphoblastic leukemia.
    Campolungo D, Salomé M, Biferali B, Tascini AS, Gabellini D., Free PMC Article

    09/22/2023
    Significance of YAP1-MAML2 rearrangement and GTF2I mutation in the diagnosis and differential diagnosis of metaplastic thymoma.

    Significance of YAP1-MAML2 rearrangement and GTF2I mutation in the diagnosis and differential diagnosis of metaplastic thymoma.
    Wang M, Xu H, Han Q, Wang L., Free PMC Article

    09/8/2023
    Unique correlation between GTF2I mutation and spindle cell morphology in thymomas (type A and AB thymomas).

    Unique correlation between GTF2I mutation and spindle cell morphology in thymomas (type A and AB thymomas).
    Wells K, Lamrca A, Papaxoinis G, Wallace A, Quinn AM, Summers Y, Nonaka D.

    06/26/2023
    Identification and validation of immune related core transcription factors GTF2I in NAFLD.

    Identification and validation of immune related core transcription factors GTF2I in NAFLD.
    Zhang M, Zhang Y, Jiao X, Lai L, Qian Y, Sun B, Yang W., Free PMC Article

    02/14/2023
    GTF2I Mutation in Thymomas: Independence From Racial-Ethnic Backgrounds. An Indian/German Comparative Study.

    GTF2I Mutation in Thymomas: Independence From Racial-Ethnic Backgrounds. An Indian/German Comparative Study.
    Jain D, Guleria P, Singh V, Parshad R, Kumar S, Gaiser T, Kurz KS, Ott G, Porubsky S, Preissler G, Sauer CG, Schölch S, Ströbel P, Hielscher T, Marx A, Popovic ZV., Free PMC Article

    03/19/2022
    Sjogren's syndrome-associated SNPs increase GTF2I expression in salivary gland cells to enhance inflammation development.

    Sjögren's syndrome-associated SNPs increase GTF2I expression in salivary gland cells to enhance inflammation development.
    Shimoyama S, Nakagawa I, Jiang JJ, Matsumoto I, Chiorini JA, Hasegawa Y, Ohara O, Hasebe R, Ota M, Uchida M, Kamimura D, Hojyo S, Tanaka Y, Atsumi T, Murakami M., Free PMC Article

    02/5/2022
    Role of the multifunctional transcription factor TFII-I in DNA damage repair.

    Role of the multifunctional transcription factor TFII-I in DNA damage repair.
    Roy AL.

    10/23/2021
    Association of GTF2I, NFKB1, and TYK2 Regional Polymorphisms With Systemic Sclerosis in a Chinese Han Population.

    Association of GTF2I, NFKB1, and TYK2 Regional Polymorphisms With Systemic Sclerosis in a Chinese Han Population.
    Liu C, Yan S, Chen H, Wu Z, Li L, Cheng L, Li H, Li Y., Free PMC Article

    09/25/2021
    Multiomics data reveals the influences of myasthenia gravis on thymoma and its precision treatment.

    Multiomics data reveals the influences of myasthenia gravis on thymoma and its precision treatment.
    Ruan X, Lu X, Gao J, Jiang L, Zhu Y, Zhou Y, Meng J, Yan H, Yan F, Wang F.

    09/11/2021
    Binding of Gtf2i-beta/delta transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro.

    Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro.
    Pan Y, Iejima D, Nakayama M, Suga A, Noda T, Kaur I, Das T, Chakrabarti S, Guymer RH, DeAngelis MM, Yamamoto M, Baird PN, Iwata T., Free PMC Article

    09/4/2021
    A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability.

    A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability.
    Pinelli M, Terrone G, Troglio F, Squeo GM, Cappuccio G, Imperati F, Pignataro P, Genesio R, Nitch L, Del Giudice E, Merla G, Testa G, Brunetti-Pierri N., Free PMC Article

    06/5/2021
    Gene of the month: GTF2I.

    Gene of the month: GTF2I.
    Nathany S, Tripathi R, Mehta A.

    01/9/2021
    TFII-I-mediated polymerase pausing antagonizes GLI2 induction by TGFbeta.

    TFII-I-mediated polymerase pausing antagonizes GLI2 induction by TGFβ.
    McCleary-Wheeler AL, Paradise BD, Almada LL, Carlson AJ, Marks DL, Vrabel A, Vera RE, Sigafoos AN, Olson RL, Fernandez-Zapico ME., Free PMC Article

    09/26/2020
    A significant genetic association in the variant rs117026326 of GTF2I and neuromyelitis optica spectrum disorder was observed in a Norther Han Chinese population.

    The GTF2I rs117026326 polymorphism is associated with neuromyelitis optica spectrum disorder but not with multiple sclerosis in a Northern Han Chinese population.
    Liang H, Gao W, Liu X, Liu J, Mao X, Yang M, Long X, Zhou Y, Zhang Q, Zhu J, Wang S, Jin T.

    06/20/2020
    TFII-I factors and the neural crest master regulator AP2alpha associate with the promoters of key genes important in the development of facial and dental structures. GTF2I and GTF2IRD1 are deleted in Williams-Beuren syndrome.

    TFII-I and AP2α Co-Occupy the Promoters of Key Regulatory Genes Associated with Craniofacial Development.
    Miranda P, Enkhmandakh B, Bayarsaihan D.

    10/12/2019
    A case-control study identified the involvement of GTF2I gene polymorphisms in development of systemic lupus erythematosus, particularly in renal involvement.

    Association of GTF2I gene polymorphisms with renal involvement of systemic lupus erythematosus in a Chinese population.
    Meng Y, He Y, Zhang J, Xie Q, Yang M, Chen Y, Wu Y., Free PMC Article

    08/17/2019
    demonstrate a marked prevalence of a thymoma-specific mutated oncogene, GTF2I

    The Integrated Genomic Landscape of Thymic Epithelial Tumors.
    Radovich M, Pickering CR, Felau I, Ha G, Zhang H, Jo H, Hoadley KA, Anur P, Zhang J, McLellan M, Bowlby R, Matthew T, Danilova L, Hegde AM, Kim J, Leiserson MDM, Sethi G, Lu C, Ryan M, Su X, Cherniack AD, Robertson G, Akbani R, Spellman P, Weinstein JN, Hayes DN, Raphael B, Lichtenberg T, Leraas K, Zenklusen JC, Cancer Genome Atlas Network, Fujimoto J, Scapulatempo-Neto C, Moreira AL, Hwang D, Huang J, Marino M, Korst R, Giaccone G, Gokmen-Polar Y, Badve S, Rajan A, Ströbel P, Girard N, Tsao MS, Marx A, Tsao AS, Loehrer PJ., Free PMC Article

    12/22/2018
    we identified largest-ever effect on Asian rheumatoid arthritis across human non-HLA regions at GTF2I by heterogeneity mapping followed by replication studies, and pinpointed a possible causal variant

    Association-heterogeneity mapping identifies an Asian-specific association of the GTF2I locus with rheumatoid arthritis.
    Kim K, Bang SY, Ikari K, Yoo DH, Cho SK, Choi CB, Sung YK, Kim TH, Jun JB, Kang YM, Suh CH, Shim SC, Lee SS, Lee J, Chung WT, Kim SK, Choe JY, Momohara S, Taniguchi A, Yamanaka H, Nath SK, Lee HS, Bae SC., Free PMC Article

    04/28/2018
    the frequency of GTF2I mutation is higher in more indolent TETs and correlated with better prognosis.

    GTF2I mutation frequently occurs in more indolent thymic epithelial tumors and predicts better prognosis.
    Feng Y, Lei Y, Wu X, Huang Y, Rao H, Zhang Y, Wang F.

    03/31/2018
    GTF2I/Gtf2i, its physiologic role in human disorders was relatively unknown until recently. Novel studies show that it is involved in an array of human diseases including neurocognitive disorders, systemic lupus erythematosus (SLE), and cancer.

    Pathophysiology of TFII-I: Old Guard Wearing New Hats.
    Roy AL., Free PMC Article

    02/10/2018
    the results reported here support a model whereby common genetic variation in GTF2I mediates human sociality and anxiety via effects on oxytocin reactivity.

    The Williams syndrome prosociality gene GTF2I mediates oxytocin reactivity and social anxiety in a healthy population.
    Procyshyn TL, Spence J, Read S, Watson NV, Crespi BJ., Free PMC Article

    02/3/2018
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