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Omics · study · 2026

Interrogating the role of a loss-of-function SETD5 mutation in hiPSC-derived astrocytes [Astrocytes_Unmerged]

Listed in NCBI GEO

Intellectual disability (ID) and autism spectrum disorder (ASD) represent a spectrum of neurodevelopmental conditions with etiology often associated with genetic variations in genes encoding chromatin regulators, such as SET-domain-containing protein 5 (SETD5).

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Here we explore the effects of a loss-of-function SETD5 variant found in a patient with ID/ASD in human induced pluripotent stem cell (hiPSC)-derived astrocytes.

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Life Sciences
Provenance · 1 source records, 8 field assertions
SourceKeyLast seenRaw
NCBI GEOGSE27807015 d agoJSON v1
FieldAssertionExtractorEvidence
access_levelsource · NCBI GEOconnector:ncbi_geo@1.0.0
concepts[field].local:field:life-sciencesmapping · NCBI GEOconnector:ncbi_geo@1.0.0
concepts[method].geo_series_type:expression-profiling-by-high-throughput-sequencingsource · NCBI GEOconnector:ncbi_geo@1.0.0/gdstype
concepts[method].geo_series_type:genome-binding-occupancy-profiling-by-high-throughput-sequencingsource · NCBI GEOconnector:ncbi_geo@1.0.0/gdstype
concepts[organism].NCBITaxon:9606source · NCBI GEOconnector:ncbi_geo@1.0.0/taxon
descriptionsource · NCBI GEOconnector:ncbi_geo@1.0.0/summary
publication_datesource · NCBI GEOconnector:ncbi_geo@1.0.0
titlesource · NCBI GEOconnector:ncbi_geo@1.0.0/title