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SIRT1 and thalassemia are reported together in 2 articles.

Gene

SIRT1

HGNC
HGNC:14929
104articles
104mentions
6variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype

Thalassemia

HPO
HP:0001878
409articles
409mentions
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

2 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
geneSIRT1“Gut microbiota-derived TMAO and SIRT1/HMGB1 Axis: unveiling mechanisms of renal impairment in beta-thalassemia major.”0.98hgnc_dict_v1
phenotypethalassemia“Gut microbiota-derived TMAO and SIRT1/HMGB1 Axis: unveiling mechanisms of renal impairment in beta-thalassemia major.”0.93phenotype_alias_lexicon_v2
geneHMGB1“Gut microbiota-derived TMAO and SIRT1/HMGB1 Axis: unveiling mechanisms of renal impairment in beta-thalassemia major.”0.98hgnc_dict_v1
TypeEntitySource evidenceConfidenceExtractor
geneSIRT1“Targeting SIRT1, NLRP3 inflammasome, and Nrf2 signaling with chrysin alleviates the iron-triggered hepatotoxicity in rats.”0.98hgnc_dict_v1
phenotypethalassemia“Blood transfusion-requiring diseases such as sickle cell anemia and thalassemia are characterized by an imbalance between iron intake and excretion, resulting in an iron overload (IOL) disorder.”0.98phenotype_alias_lexicon_v2
geneNLRP3“Targeting SIRT1, NLRP3 inflammasome, and Nrf2 signaling with chrysin alleviates the iron-triggered hepatotoxicity in rats.”0.98hgnc_dict_v1
phenotypesickle cell anemia“Blood transfusion-requiring diseases such as sickle cell anemia and thalassemia are characterized by an imbalance between iron intake and excretion, resulting in an iron overload (IOL) disorder.”0.98phenotype_alias_lexicon_v2