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Omics · study · 2026

Erythroid ACKR1 deficiency aggravates immune-mediated kidney disease

Listed in NCBI GEO

Single nucleotide polymorphisms (SNP) of atypical chemokine receptor 1 (ACKR1) gene encode human Duffy Antigen blood groups.

Description

The majority of individuals of West African ancestry carry a SNP in the promoter region of the ACKR1 that disrupts its transcription in erythroid cells only, but not in venular endothelial cells, leading to an “erythroid silent”, FyBES Duffy phenotype.Irradiation bone marrow ACKR1 chimeric mice lacking erythroid ACKR1 (KO->WT) showed increased disease activity and fibrosis after induction of nephrotoxic serum nephritis (NTSN), as compared to their respective controls (WT->WT).

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From keywords
Life Sciences
Inferred from text
Disease 75%
Provenance · 1 source records, 8 field assertions
SourceKeyLast seenRaw
NCBI GEOGSE27601715 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].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