<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Prof.GangLi, faculty of health and science, university of macau</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA399160</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Lysine27Methionine mutations (K27M) in the histone H3 (H3.3 and H3.1) are highly prevalent in pediatric high-grade gliomas (HGG). This study found H3.3K27M caused the upregulation of multiple cancer/testis (CT) antigens, include IL13RA2 and VCX family proteins. Overexpression of VCX3A/B stimulates the expression of genes involved in immune response. Overall design: Total RNA was extracted from Res259 cells stably expressing H3.3K27M, pCMV6-Entry (empty vector), different forms of GFP-VCX3A/B, or GFP (as control), and subjected to an Illumina HT12.2 Bead CHIP array analysis.</long_description><tag>xref:PubMed:29453317</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>Histone H3.3K27M mutation activates multiple cancer/testis antigens</description><dates><last_updated>2025-09-24</last_updated><first_public>2018-08-02</first_public></dates><accession>PRJNA399160</accession><cross_references><GEO>GSE102886</GEO><taxon>9606</taxon><PubMed>29453317</PubMed></cross_references></HashMap>