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CALM3 and long QT syndrome are reported together in 1 article.

Gene

CALM3

HGNC
HGNC:1449
1articles
1mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
44articles
44mentions
10co-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

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry.

PMID 31170290 | PMCID PMC6748747 | DOI 10.1093/eurheartj/ehz311 · European heart journal · 2019 · 5 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneCALM3“ICalmR has enrolled 74 subjects, with a variant in the CALM1 (n = 36), CALM2 (n = 23), or CALM3 (n = 15) genes.”0.98hgnc_dict_v1
phenotypelong QT syndrome“The two prevalent phenotypes are long QT syndrome (LQTS; CALM-LQTS, n = 36, 49%) and catecholaminergic polymorphic ventricular tachycardia (CPVT; CALM-CPVT, n = 21, 28%).”0.98phenotype_alias_lexicon_v2
geneCALM1“ICalmR has enrolled 74 subjects, with a variant in the CALM1 (n = 36), CALM2 (n = 23), or CALM3 (n = 15) genes.”0.98hgnc_dict_v1
geneCALM2“ICalmR has enrolled 74 subjects, with a variant in the CALM1 (n = 36), CALM2 (n = 23), or CALM3 (n = 15) genes.”0.98hgnc_dict_v1