Identity
HGNC
LOCATION
19q13.32
LOCUSID
ALIAS
CALM,CAM1,CAM2,CAMB,CPVT6,CaM,CaMIII,HEL-S-72,LQT16,PHKD,PHKD3
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 808
MIM: 114183
HGNC: 1449
Ensembl: ENSG00000160014
Variants:
dbSNP: 808
ClinVar: 808
TCGA: ENSG00000160014
COSMIC: CALM3
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37380439 | 2023 | Calmodulinopathy in Japanese Children - Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy. | 0 |
| 37932969 | 2023 | CALM3 affects the prognosis of leukemia and hemorrhoids. | 0 |
| 37380439 | 2023 | Calmodulinopathy in Japanese Children - Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy. | 0 |
| 37932969 | 2023 | CALM3 affects the prognosis of leukemia and hemorrhoids. | 0 |
| 35225649 | 2022 | Novel CALM3 Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation Family. | 9 |
| 35225649 | 2022 | Novel CALM3 Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation Family. | 9 |
| 33191766 | 2020 | Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative CALM1-3 Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death Victims. | 1 |
| 33191766 | 2020 | Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative CALM1-3 Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death Victims. | 1 |
| 31454269 | 2019 | Genetic Mosaicism in Calmodulinopathy. | 20 |
| 31454269 | 2019 | Genetic Mosaicism in Calmodulinopathy. | 20 |
| 28744816 | 2018 | ACE2, CALM3 and TNNI3K polymorphisms as potential disease modifiers in hypertrophic and dilated cardiomyopathies. | 14 |
| 29606593 | 2018 | A Mechanism of Calmodulin Modulation of the Human Cardiac Sodium Channel. | 34 |
| 29932249 | 2018 | Protein phenotype diagnosis of autosomal dominant calmodulin mutations causing irregular heart rhythms. | 5 |
| 28744816 | 2018 | ACE2, CALM3 and TNNI3K polymorphisms as potential disease modifiers in hypertrophic and dilated cardiomyopathies. | 14 |
| 29606593 | 2018 | A Mechanism of Calmodulin Modulation of the Human Cardiac Sodium Channel. | 34 |
Citation
Dessen P
CALM3 (calmodulin 3)
Atlas Genet Cytogenet Oncol Haematol. 2013-03-01
Online version: http://atlasgeneticsoncology.org/gene/53209/calm3
