Advanced search

Combine gene, variant, phenotype, region and year filters

Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

Transparent by designEvery result links extracted entities to its source sentence and publication identifier.
About your search

CXCL8 and renal failure are reported together in 1 article.

Gene

CXCL8

HGNC
HGNC:6025
24articles
24mentions
2variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype

Renal failure

523articles
523mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

1 records shown · first 60

Identification of pathogenic genes associated with CKD: An integrated bioinformatics approach.

PMID 36035163 | PMCID PMC9403320 | DOI 10.3389/fgene.2022.891055 · Frontiers in genetics · 2022 · 7 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneCXCL8“After sub-network analysis we identified six overlapped hub genes (RPS5, RPL37A, RPLP0, CXCL8, HLA-A, and ANXA1).”0.98hgnc_dict_v1
phenotyperenal failure“Identification of pathogenic genes associated with CKD: An integrated bioinformatics approach.”0.93phenotype_alias_lexicon_v2
geneRPS5“After sub-network analysis we identified six overlapped hub genes (RPS5, RPL37A, RPLP0, CXCL8, HLA-A, and ANXA1).”0.98hgnc_dict_v1
geneRPL37A“After sub-network analysis we identified six overlapped hub genes (RPS5, RPL37A, RPLP0, CXCL8, HLA-A, and ANXA1).”0.98hgnc_dict_v1