<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/GSE278nnn/GSE278313/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE278313</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Cryptic splice sites generate heterogeneous EZH2 isoforms with distinct functions in embryonic development [CUT&amp;Tag]</name><description>A novel Ezh2 variant was identified, we named Ezh2b, which is lost 27-nt region in the end of exon3, has different functions on embryonic development in mouse compared to Ezh2 with 27-nt region (namely as Ezh2a). Here, we apply transcriptome sequencing to explore the underlying molecular mechanisms.</description><dates><publication>2025/09/17</publication></dates><accession>GSE278313</accession><cross_references><GSM>GSM8544669</GSM><GSM>GSM8544668</GSM><GSM>GSM8544679</GSM><GSM>GSM8544667</GSM><GSM>GSM8544678</GSM><GSM>GSM8544677</GSM><GSM>GSM8544666</GSM><GSM>GSM8544672</GSM><GSM>GSM8544661</GSM><GSM>GSM8544671</GSM><GSM>GSM8544670</GSM><GSM>GSM8544680</GSM><GSM>GSM8544665</GSM><GSM>GSM8544676</GSM><GSM>GSM8544664</GSM><GSM>GSM8544675</GSM><GSM>GSM8544674</GSM><GSM>GSM8544663</GSM><GSM>GSM8544662</GSM><GSM>GSM8544673</GSM><GPL>24247</GPL><GSE>278313</GSE><taxon>Mus musculus</taxon><PMID>[40923763]</PMID></cross_references></HashMap>