{"database":"ENA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["University of Edinburgh"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA878466"],"long_description":["This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series"],"repository":["ENA"],"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"],"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"],"additional_accession":[]},"is_claimable":false,"name":"Mutation of ATRX induces type I interferon signalling and defines a non-canonical role of nuclear cGAS in the regulation of chromatin state","description":"Mutation of ATRX induces type I interferon signalling and defines a non-canonical role of nuclear cGAS in the regulation of chromatin state","dates":{"last_updated":"2025-09-24","first_public":"2023-09-28"},"accession":"PRJNA878466","cross_references":{"GEO":["GSE212923"]}}