Gene
CALM2
calmodulin 2
- HGNC 1445↗(opens in a new tab)
- Ensembl gene ENSG00000143933↗(opens in a new tab)
- NCBI Gene 805↗(opens in a new tab)
Summary
- Cytogenetic location
- 2p21
- Coordinates
- Chromosome 2: 47,160,084–47,176,511 (GRCh38)
- Exons
- 6 exons across 16.4 kb
- Protein
- 149 amino acids
- Also known as
- PHKD, PHKD2, CAMII
- MANE Select transcript
- ENST00000272298.12NM_001743.6
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome TestCurated reports relevant to this gene
Catecholaminergic Polymorphic Ventricular Tachycardia
- Ventricular Tachycardia, Familial
An instance of ventricular tachycardia that is caused by an inherited modification of the individual's genome.
- ClinGen rates the link moderate
- 1 GenCC submitter rates it definitive or strong
- Polymorphic Ventricular Tachycardia
A ventricular tachycardia that is irregular in rate and rhythm.
- ClinGen rates the link moderate
- 1 GenCC submitter rates it definitive or strong
Long QT Syndrome
A disorder of cardiac repolarisation marked by a prolonged QT interval and a risk of dangerous ventricular arrhythmias such as torsades de pointes.
- ClinGen rates the link definitive
- 3 GenCC submitters rate it definitive or strong
- On the ACMG secondary findings list
What knowing changes
Beta-blockers, ICD placement, activity restriction, genetic counseling
How CALM2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 1.2 kb of the gene's 16.4 kb; 450 of those bases code for the protein.
How a genome test reads CALM2
17
positions in CALM2 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 16.4 kb of CALM2, introns included, not only the 1.2 kb of exons.
Genes linked to the same conditions
- CALM1calmodulin 1Shares 3 conditions
- CALM3calmodulin 3Shares 3 conditions
- TRDNtriadinShares 3 conditions
- CASQ2calsequestrin 2Shares 2 conditions
- RYR2ryanodine receptor 2Shares 2 conditions
- TECRLtrans-2,3-enoyl-CoA reductase likeShares 2 conditions
- CACNA1Ccalcium voltage-gated channel subunit alpha1 CShares 1 condition
- KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1Shares 1 condition
- KCNH2potassium voltage-gated channel subfamily H member 2Shares 1 condition
- KCNJ2potassium inwardly rectifying channel subfamily J member 2Shares 1 condition
- KCNQ1potassium voltage-gated channel subfamily Q member 1Shares 1 condition
- SCN5Asodium voltage-gated channel alpha subunit 5Shares 1 condition
Traits linked to CALM2
The Human Phenotype Ontology lists these as features of the rare conditions CALM2 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). CALM2 gene: calmodulin 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/calm2
Dante Labs. CALM2 gene: calmodulin 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/calm2
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