CALM2 (calmodulin 2)

Gene
Gene SNPs Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
805
Gene name Gene Name - the full gene name approved by the HGNC.
Calmodulin 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CALM2
Synonyms (NCBI Gene) Gene synonyms aliases
CALM, CALML2, CAM1, CAM3, CAMC, CAMII, CAMIII, LQT15, PHKD, PHKD2, caM
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p21
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the calmodulin gene family. There are three distinct calmodulin genes dispersed throughout the genome that encode the identical protein, but differ at the nucleotide level. Calmodulin is a calcium binding protein that plays a role
miRNA miRNA information provided by mirtarbase database.
Gene SNPs Other IDs Associated diseases
Show/Hide all(696)
miRTarBase ID miRNA Experiments Reference
MIRT005904 hsa-miR-1-3p qRT-PCR 21169019
MIRT005904 hsa-miR-1-3p Proteomics 18668040
MIRT040483 hsa-miR-598-3p CLASH 23622248
MIRT507911 hsa-miR-130a-3p HITS-CLIP 21572407
MIRT507910 hsa-miR-3666 HITS-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene SNPs Other IDs Associated diseases
Show/Hide all(86)
GO ID Ontology Definition Evidence Reference
GO:0000086 Process G2/M transition of mitotic cell cycle IEA
GO:0000922 Component Spindle pole IDA 16760425
GO:0000922 Component Spindle pole IEA
GO:0002027 Process Regulation of heart rate IEA
GO:0002027 Process Regulation of heart rate IMP 23040497
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene SNPs Other IDs Associated diseases
MIM HGNC e!Ensembl
114182 1445 ENSG00000143933
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene SNPs Other IDs Associated diseases
Show/Hide Causal Diseases (1)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Long QT Syndrome long qt syndrome 1, long qt syndrome 15, long qt syndrome rs730882254, rs398124647, rs1553431702, rs1558693760, rs1573214371, rs398124648, rs1573214163, rs398124650, rs398124649 N/A
Show/Hide Text Mining Associations (28)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 31984950
Arrhythmias Cardiac Associate 23388215, 24917665, 31170290, 37528649
Atrioventricular Block Associate 27374306
Bradycardia Associate 27374306
Breast Neoplasms Associate 26458823
Channelopathies Associate 35543671, 37622577
Death Associate 21546767, 27100291
Death Sudden Associate 31170290, 37380439
Death Sudden Cardiac Associate 27100291
Diabetes Mellitus Type 2 Associate 21546767