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Omics · study · 2026

Epigenetic alterations of the imprinted SLC22A18 gene contributed to congenital "Allergy-Short-stature-fatty liver" syndrome by via β-catenin-Ascl2 axis

Listed in NCBI GEO

Epigenetic syndrome is a multisystem, eternal, and devastating disease associated with imprinted gene variants.

Description

Our previous study showed a strong correlation between the SLC22A18 and the "Allergy-Short stature-fatty liver" (ASFL) syndrome in children. However, the mechanisms by which SLC22A18 influences ASFL syndrome remain unknown.SLC22A18 deficiency also induced higher lipid accumulation in liver in the mouse model.

Whether SLC22A18 deletion promotes hepatic steatosis deserves further investigation.

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From keywords
Life Sciences
Inferred from text
Disease 75% · Genetics 73%
Provenance · 1 source records, 9 field assertions
SourceKeyLast seenRaw
NCBI GEOGSE32248713 d agoJSON v1
FieldAssertionExtractorEvidence
access_levelsource · NCBI GEOconnector:ncbi_geo@1.0.0
concepts[disease].local:disease:diseaseenrichment · NCBI GEOkeyword-concept-rules@1.0.0title+description (75%)
concepts[field].anzsrc:group:3105enrichment · NCBI GEOtaxonomy-embedding@1.1.0title+keywords+description (73%)
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[organism].NCBITaxon:10090source · 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