Genetic Syndromes and Imprinting
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Scope of this subject
This cluster of papers explores the phenomenon of genomic imprinting, where certain genes are expressed in a parent-of-origin-specific manner. It covers topics such as parental influence on gene expression, epigenetic regulation through DNA methylation, and the role of imprinted genes in syndromes like Prader-Willi and Angelman. Additionally, it delves into the mechanisms of imprint control regions and the involvement of non-coding RNA in regulating imprinted gene networks.
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Research vocabulary
genomic imprinting; Prader-Willi syndrome; Angelman syndrome; Beckwith-Wiedemann syndrome; imprinted genes; Silver-Russell syndrome; H19; monoallelic expression; uniparental disomy; imprinting control regions; UBE3A; chromosome 15q11-q13; loss of imprinting; imprinting disorders; SNRPN; Sotos syndrome; overgrowth syndromes; parent-of-origin gene expression; paternal uniparental disomy; CDKN1C; maternal uniparental disomy; biallelic expression; paternally expressed genes; parent-of-origin effects; IGF2R
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Morton address: 36183297730864711 · morton4x16-v1
Coordinates: (1, 13, 1311, 11928). The address interleaves categorical identifier bits. Nearby addresses are not guaranteed to describe semantically similar subjects.
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