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CYP51A1 and Crohn disease are reported together in 1 article.

HGNC
HGNC:2649
6articles
6mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
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
geneCYP51A1“In inflamed Crohn's ileum, CYP3A4, CYP20A1, CYP51A1, ADH1B, ALPI, FOM1, SULT1A2, SULT1B1 and ABCB7 showed ≥10-fold reduction in abundance compared with healthy baseline.”0.98hgnc_dict_v1
phenotypeCrohn disease“Quantitative Assessment of the Impact of Crohn's Disease on Protein Abundance of Human Intestinal Drug-Metabolising Enzymes and Transporters.”0.93phenotype_alias_lexicon_v2
geneCYP3A4“In inflamed Crohn's ileum, CYP3A4, CYP20A1, CYP51A1, ADH1B, ALPI, FOM1, SULT1A2, SULT1B1 and ABCB7 showed ≥10-fold reduction in abundance compared with healthy baseline.”0.98hgnc_dict_v1
geneCYP20A1“In inflamed Crohn's ileum, CYP3A4, CYP20A1, CYP51A1, ADH1B, ALPI, FOM1, SULT1A2, SULT1B1 and ABCB7 showed ≥10-fold reduction in abundance compared with healthy baseline.”0.98hgnc_dict_v1