<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE314nnn/GSE314187/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE314187</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Bulk RNAseq of MRGPRX4+/+ and MRGPRX4-/- A2058 human melanoma cells</name><description>This study investigates the transcriptional consequences of loss of the Mas-related G protein?coupled receptor MRGPRX4 in human melanoma cells. Bulk RNA sequencing was performed on CRISPR-Cas9-engineered MRGPRX4 knockout and control A2058 melanoma cell lines. Sequencing data were processed using established RNA-seq workflows, including quality control and transcript quantification, followed by differential gene expression and functional enrichment analyses to identify gene expression programs regulated by MRGPRX4.</description><dates><publication>2026/09/15</publication></dates><accession>GSE314187</accession><cross_references><GSM>GSM9383732</GSM><GSM>GSM9383733</GSM><GSM>GSM9383726</GSM><GSM>GSM9383727</GSM><GSM>GSM9383728</GSM><GSM>GSM9383729</GSM><GSM>GSM9383730</GSM><GSM>GSM9383731</GSM><GPL>24676</GPL><GSE>314187</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>