<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>University of Edinburgh</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA878466</full_dataset_link><long_description>This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series</long_description><repository>ENA</repository><description_synonyms>nuclear chromatin, Regulations, cytoplasmic chromatin, biological signaling, X-linked, Formal Social Control, ATR2, Alpha thalassemia mental retardation syndrome, Alpha thalassemia intellectual disability syndrome, ALPHA-thalassemia/mental retardation syndrome, Xnp, XNP, Social Controls, SHS, 4833408C14Rik, Concept, Mutations, Alpha-thalassemia/intellectual disability syndrome, ATRX, Role Concept, XLMR hypotonic face syndrome, nondeletion type, HP1-BP38, Roles, Social Control, MRXS3, Role, Alpha-thalassemia/mental retardation syndrome, SFM1, Concepts, Type I, interferon type I, Alpha-thalassemia-X-linked intellectual disability syndrome, ATRX syndrome, Formal Social Controls, Chromatins, XH2, Nondeletion type, Interferons, chromosome scaffold., IFN type I, Interferons Type I, MRXHF1, Control, ZNF-HX, RAD54L, Controls, signalling, Social, DXHXS6677E, ALPHA-thalassemia/intellectual disability syndrome, AI447451, Hp1bp2, Rad54, signalling process, Type I Interferon, Alpha-thalassemia X-linked intellectual disability syndrome, Type I Interferons, signaling process, Role Concepts, JMS, regulation, RAD54, Interferon, Regulation, Hp1bp38, single organism signaling, ATR</description_synonyms><name_synonyms>nuclear chromatin, Regulations, cytoplasmic chromatin, biological signaling, X-linked, Formal Social Control, ATR2, Alpha thalassemia mental retardation syndrome, Alpha thalassemia intellectual disability syndrome, ALPHA-thalassemia/mental retardation syndrome, Xnp, XNP, Social Controls, SHS, 4833408C14Rik, Concept, Mutations, Alpha-thalassemia/intellectual disability syndrome, ATRX, Role Concept, XLMR hypotonic face syndrome, nondeletion type, HP1-BP38, Roles, Social Control, MRXS3, Role, Alpha-thalassemia/mental retardation syndrome, SFM1, Concepts, Type I, interferon type I, Alpha-thalassemia-X-linked intellectual disability syndrome, ATRX syndrome, Formal Social Controls, Chromatins, XH2, Nondeletion type, Interferons, chromosome scaffold., IFN type I, Interferons Type I, MRXHF1, Control, ZNF-HX, RAD54L, Controls, signalling, Social, DXHXS6677E, ALPHA-thalassemia/intellectual disability syndrome, AI447451, Hp1bp2, Rad54, signalling process, Type I Interferon, Alpha-thalassemia X-linked intellectual disability syndrome, Type I Interferons, signaling process, Role Concepts, JMS, regulation, RAD54, Interferon, Regulation, Hp1bp38, single organism signaling, ATR</name_synonyms></additional><is_claimable>false</is_claimable><name>Mutation of ATRX induces type I interferon signalling and defines a non-canonical role of nuclear cGAS in the regulation of chromatin state</name><description>Mutation of ATRX induces type I interferon signalling and defines a non-canonical role of nuclear cGAS in the regulation of chromatin state</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-09-28</first_public></dates><accession>PRJNA878466</accession><cross_references><GEO>GSE212923</GEO></cross_references></HashMap>