Human Gene Set: GOBP_FACULTATIVE_HETEROCHROMATIN_FORMATION

For the Mouse gene set with the same name, see GOBP_FACULTATIVE_HETEROCHROMATIN_FORMATION

Standard name GOBP_FACULTATIVE_HETEROCHROMATIN_FORMATION
Systematic name M42990
Brief description The compaction of chromatin into a conformation that is refactory to transcription but that be converted to euchromatin and allow transcription in specific contexts. These can be temporal (e.g., developmental states or specific cell-cycle stages), spatial (e.g., nuclear localization changes from the center to the periphery or vice versa due to exogenous factors/signals), or parental/heritable (e.g., monoallelic gene expression). [PMID:17936700]
Full description or abstract  
Collection C5: Ontology
      GO: Gene Ontology
            GO:BP: GO Biological Process
Source publication  
Exact source GO:0140718
Related gene sets  
External links http://amigo.geneontology.org/amigo/term/GO:0140718
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Source species Homo sapiens
Contributed by Gene Ontology (Gene Ontology Consortium)
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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Version history 2024.1.Hs: Updated to GO Release 2024-04-24.

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