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CXCL8 and Crohn disease 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

Crohn disease

435articles
435mentions
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
TypeEntitySource evidenceConfidenceExtractor
geneCXCL8“XGBoost classification achieved an overall accuracy of 88% (IBD: 71%, controls: 93%), with SHAP analysis pinpointing nine key genes, including AQP9, CXCL8, IFITM1, and ITGA5.”0.98hgnc_dict_v1
phenotypeCrohn disease“RNA-sequencing data (GSE165512) from 170 samples-84 Crohn's disease (CD), 40 ulcerative colitis (UC), and 46 controls-were normalized using R.”0.93phenotype_alias_lexicon_v2
geneAQP9“AQP9 and IFITM1 as drivers of immune infiltration and tumor progression in IBD-associated colorectal cancer: from computational insights to experimental validation.”0.98hgnc_dict_v1
geneIFITM1“AQP9 and IFITM1 as drivers of immune infiltration and tumor progression in IBD-associated colorectal cancer: from computational insights to experimental validation.”0.98hgnc_dict_v1