U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination
    • Showing Current items.

    ZNF202 zinc finger protein 202 [ Homo sapiens (human) ]

    Gene ID: 7753, updated on 5-Mar-2024

    GeneRIFs: Gene References Into Functions

    Submit: New GeneRIFCorrection

    GeneRIFPubMed TitleDate
    Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)

    Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
    Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S, DREAM investigators., Free PMC Article

    		09/15/2010
    Observational study and genome-wide association study of gene-disease association. (HuGE Navigator)

    Genomewide association study of movement-related adverse antipsychotic effects.
    Aberg K, Adkins DE, Bukszár J, Webb BT, Caroff SN, Miller DD, Sebat J, Stroup S, Fanous AH, Vladimirov VI, McClay JL, Lieberman JA, Sullivan PF, van den Oord EJ., Free PMC Article

    		12/2/2009
    SOX17-Chromatin immunoprecipitation identified zinc finger protein 202 (Zfp202) as a direct target of SOX17 during endoderm differentiation of F9 embryonal carcinoma cells.

    SOX17 directly activates Zfp202 transcription during in vitro endoderm differentiation.
    Patterson ES, Addis RC, Shamblott MJ, Gearhart JD.

    		01/21/2010
    Homozygosity for a common functional promoter variant in ZNF202 predicts severe atherosclerosis and an increased risk of IHD.

    Functional promoter variant in zinc finger protein 202 predicts severe atherosclerosis and ischemic heart disease.
    Stene MC, Frikke-Schmidt R, Nordestgaard BG, Grande P, Schnohr P, Tybjaerg-Hansen A.

    		01/21/2010
    Observational study of gene-disease association. (HuGE Navigator)See all PubMed (5) articles

    Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
    Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD, ASCOT investigators, NORDIL investigators, BRIGHT Consortium.

    Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.
    Drenos F, Talmud PJ, Casas JP, Smeeth L, Palmen J, Humphries SE, Hingorani AD.

    Zinc Finger Protein 202, genetic variation, and HDL cholesterol in the general population.
    Stene MC, Frikke-Schmidt R, Nordestgaard BG, Tybjaerg-Hansen A, Stene MC, Frikke-Schmidt R, Nordestgaard BG, Tybjaerg-Hansen A.

    High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts.
    Park JW, Cai J, McIntosh I, Jabs EW, Fallin MD, Ingersoll R, Hetmanski JB, Vekemans M, Attie-Bitach T, Lovett M, Scott AF, Beaty TH.

    Zinc Finger Protein 202: a new candidate gene for ischemic heart disease: The Copenhagen City Heart Study.
    Stene MC, Frikke-Schmidt R, Nordestgaard BG, Steffensen R, Schnohr P, Tybjaerg-Hansen A, Stene MC, Frikke-Schmidt R, Nordestgaard BG, Steffensen R, Schnohr P, Tybjaerg-Hansen A.

    		03/13/2008
    findings show that genetic variation in ZNF202 is common in the general population. However, SNPs in the protein-coding region of ZNF202 do not make a major contribution to HDL cholesterol levels.

    Zinc Finger Protein 202, genetic variation, and HDL cholesterol in the general population.
    Stene MC, Frikke-Schmidt R, Nordestgaard BG, Tybjaerg-Hansen A, Stene MC, Frikke-Schmidt R, Nordestgaard BG, Tybjaerg-Hansen A.

    		01/21/2010
    This is the first study to suggest that ZNF202 could be a new candidate gene for ischemic heart disease and myocardial infarction in the general population.

    Zinc Finger Protein 202: a new candidate gene for ischemic heart disease: The Copenhagen City Heart Study.
    Stene MC, Frikke-Schmidt R, Nordestgaard BG, Steffensen R, Schnohr P, Tybjaerg-Hansen A, Stene MC, Frikke-Schmidt R, Nordestgaard BG, Steffensen R, Schnohr P, Tybjaerg-Hansen A.

    		01/21/2010
    firstprevious page of 1 nextlast