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TERT and leukemia are reported together in 2 articles.

Gene

TERT

HGNC
HGNC:11730
48articles
48mentions
2variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype

Leukemia

652articles
652mentions
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

Transcriptomic Analysis of Conserved Telomere Maintenance Component 1 (CTC1) and Its Association with Leukemia.

PMID 36233645 | PMCID PMC9571731 | DOI 10.3390/jcm11195780 · Journal of clinical medicine · 2022 · 4 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneTERT“Telomere length (TEL) regulation is important for genome stability and is governed by the coordinated role of shelterin proteins, telomerase (TERT), and CST (CTC1/OBFC1/TEN1) complex.”0.98hgnc_dict_v1
phenotypeleukemia“Transcriptomic Analysis of Conserved Telomere Maintenance Component 1 (CTC1) and Its Association with Leukemia.”0.98phenotype_alias_lexicon_v2
geneCTC1“Transcriptomic Analysis of Conserved Telomere Maintenance Component 1 (CTC1) and Its Association with Leukemia.”0.98hgnc_dict_v1
geneTEN1“Telomere length (TEL) regulation is important for genome stability and is governed by the coordinated role of shelterin proteins, telomerase (TERT), and CST (CTC1/OBFC1/TEN1) complex.”0.98hgnc_dict_v1

Epithelial Cell Adhesion Molecule (EpCAM) Expression Can Be Modulated via NFκB.

PMID 36428553 | PMCID PMC9687693 | DOI 10.3390/biomedicines10112985 · Biomedicines · 2022 · 2 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneTERT“Expression of EpCAM and its downstream target genes (Myc and TERT) wasdownregulated upon treatment with costunolide in Jurkat cells.”0.98hgnc_dict_v1
phenotypeleukemia“In the current research study, qPCR induced expression of EpCAM was noted in acute lymphoblastic leukemia (ALL) cases.”0.98phenotype_alias_lexicon_v2