Catecholaminergic polymorphic ventricular tachycardia 4

disease
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Also known as CALM1 catecholaminergic polymorphic ventricular tachycardiacatecholaminergic polymorphic ventricular tachycardia caused by mutation in CALM1catecholaminergic polymorphic ventricular tachycardia type 4CPVT4ventricular tachycardia, catecholaminergic polymorphic, 4ventricular tachycardia, catecholaminergic polymorphic, type 4

Summary

Catecholaminergic polymorphic ventricular tachycardia 4 (MONDO:0013966) is a disease caused by CALM1 (GenCC Strong), with 1 cohort gene.

At a glance

  • Causal gene: CALM1 (GenCC Strong)
  • Cohort genes: 1
  • ClinVar variants: 128

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namecatecholaminergic polymorphic ventricular tachycardia 4
Mondo IDMONDO:0013966
OMIM614916
DOIDDOID:0060678
UMLSC3554047
MedGen766961
GARD0015880
Is cancer (heuristic)no

Also known as: CALM1 catecholaminergic polymorphic ventricular tachycardia · catecholaminergic polymorphic ventricular tachycardia 4 · catecholaminergic polymorphic ventricular tachycardia caused by mutation in CALM1 · catecholaminergic polymorphic ventricular tachycardia type 4 · CPVT4 · ventricular tachycardia, catecholaminergic polymorphic, 4 · ventricular tachycardia, catecholaminergic polymorphic, type 4

Data availability: 128 ClinVar variants · 3 GenCC gene-disease records.

Disease family

Classification path: disease › human disease › disease by body system or component › cardiovascular disorderheart disorderheart conduction diseasecatecholaminergic polymorphic ventricular tachycardiacatecholaminergic polymorphic ventricular tachycardia 4

Related subtypes (6): catecholaminergic polymorphic ventricular tachycardia 1, catecholaminergic polymorphic ventricular tachycardia 2, catecholaminergic polymorphic ventricular tachycardia 3, catecholaminergic polymorphic ventricular tachycardia 5, long QT syndrome 16, ventricular tachycardia, catecholaminergic polymorphic 6

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

ClinVar germline variants

128 retrieved; paginated sample, class counts are floors:

83 likely benign, 21 uncertain significance, 8 pathogenic, 6 benign, 5 benign/likely benign, 2 conflicting classifications of pathogenicity, 2 likely pathogenic, 1 pathogenic/likely pathogenic

ClinVarVariant (HGVS)GeneClassificationReview
1362982NM_006888.6(CALM1):c.395A>G (p.Asp132Gly)CALM1Pathogeniccriteria provided, single submitter
2100843NM_006888.6(CALM1):c.286G>T (p.Asp96Tyr)CALM1Pathogeniccriteria provided, single submitter
39758NM_006888.6(CALM1):c.293A>G (p.Asn98Ser)CALM1Pathogenic/Likely pathogeniccriteria provided, multiple submitters, no conflicts
426161NM_006888.6(CALM1):c.424T>C (p.Phe142Leu)CALM1Pathogeniccriteria provided, multiple submitters, no conflicts
4785412NM_006888.6(CALM1):c.270C>G (p.Phe90Leu)CALM1Pathogeniccriteria provided, single submitter
4787824NM_006888.6(CALM1):c.389A>T (p.Asp130Val)CALM1Pathogeniccriteria provided, single submitter
639902NM_006888.6(CALM1):c.394G>A (p.Asp132Asn)CALM1Pathogeniccriteria provided, single submitter
948239NM_006888.6(CALM1):c.395A>T (p.Asp132Val)CALM1Pathogeniccriteria provided, single submitter
961658NM_006888.6(CALM1):c.426C>A (p.Phe142Leu)CALM1Pathogeniccriteria provided, single submitter
39757NM_006888.6(CALM1):c.161A>T (p.Asn54Ile)CALM1Likely pathogeniccriteria provided, single submitter
542137NM_006888.6(CALM1):c.398G>A (p.Gly133Glu)CALM1Likely pathogeniccriteria provided, single submitter
1086423NM_006888.6(CALM1):c.4-9T>ACALM1Conflicting classifications of pathogenicitycriteria provided, conflicting classifications
3826954NM_006888.6(CALM1):c.4-4A>GCALM1Conflicting classifications of pathogenicitycriteria provided, conflicting classifications
1062650NC_000014.8:g.(?90870713)(90871071_?)dupCALM1Uncertain significancecriteria provided, single submitter
1424459NM_006888.6(CALM1):c.328A>C (p.Met110Leu)CALM1Uncertain significancecriteria provided, single submitter
1718023NM_006888.6(CALM1):c.358G>A (p.Glu120Lys)CALM1Uncertain significancecriteria provided, multiple submitters, no conflicts
1740325NM_006888.6(CALM1):c.4-3T>CCALM1Uncertain significancecriteria provided, multiple submitters, no conflicts
2061992NM_006888.6(CALM1):c.70G>A (p.Gly24Ser)CALM1Uncertain significancecriteria provided, single submitter
2132986NM_006888.6(CALM1):c.402C>G (p.Asp134Glu)CALM1Uncertain significancecriteria provided, single submitter
2425651NC_000014.8:g.(?90863575)(90871061_?)dupCALM1Uncertain significancecriteria provided, single submitter
2953702NM_006888.6(CALM1):c.398G>C (p.Gly133Ala)CALM1Uncertain significancecriteria provided, single submitter
3244035NC_000014.8:g.(?90863575)(90871061_?)delCALM1Uncertain significancecriteria provided, single submitter
3748203NM_006888.6(CALM1):c.154A>G (p.Met52Val)CALM1Uncertain significancecriteria provided, single submitter
3756961NM_006888.6(CALM1):c.35-12_35-11delinsCCCALM1Uncertain significancecriteria provided, single submitter
3759214NM_006888.6(CALM1):c.199C>T (p.Pro67Ser)CALM1Uncertain significancecriteria provided, single submitter
3759522NM_006888.6(CALM1):c.35-44_77dupCALM1Uncertain significancecriteria provided, single submitter
3759525NM_006888.6(CALM1):c.293A>T (p.Asn98Ile)CALM1Uncertain significancecriteria provided, single submitter
3902818NM_006888.6(CALM1):c.133A>G (p.Thr45Ala)CALM1Uncertain significancecriteria provided, single submitter
475380NM_006888.6(CALM1):c.157A>G (p.Ile53Val)CALM1Uncertain significancecriteria provided, single submitter
4785968NM_006888.6(CALM1):c.178+4A>CCALM1Uncertain significancecriteria provided, single submitter

Genes & proteins

Mendelian disease overlap and somatic drivers

GenCC: 7 · Orphanet: 2 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0

GenCC gene–disease validity (cohort genes)

the Disease column is the GenCC-asserted condition — a cohort gene’s strongest validity may be for a related predisposition syndrome.

GeneClassificationInheritanceDiseaseRecords
CALM1StrongAutosomal dominantcatecholaminergic polymorphic ventricular tachycardia 47

Orphanet rare-disease linkage (cohort genes)

GeneOrphanet IDRare disease
CALM1Orphanet:101016Romano-Ward syndrome
CALM1Orphanet:3286Catecholaminergic polymorphic ventricular tachycardia

Cohort genes → proteins

1 cohort genes, 1 distinct canonical proteins.

Evidence partition

SubsetGenes
multi_evidence1

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
CALM1HGNC:1442ENSG00000198668P0DP23Calmodulin-1gencc,clinvar

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
CALM1Calmodulin-1Calmodulin acts as part of a calcium signal transduction pathway by mediating the control of a large number of enzymes, ion channels, aquaporins and other proteins through calcium-binding.

Protein-family classification

Druggable: 0 · Difficult: 0 · Unknown: 1 · Druggable fraction: 0.0

Family distribution

Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.

FamilyGenesFoldFDR
Other/Unknown11.8×0.558

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
CALM1Other/UnknownnoEF_hand_dom, EF-hand-dom_pair, EF_Hand_1_Ca_BS

Expression context

Cohort genes with no expression data: 0.

1 cohort gene are a single-cell marker in ≥1 SCXA experiment.

Breadth distribution (Bgee present_calls)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)1
unknown0

Top tissues across cohort

TissueCohort genes
lateral nuclear group of thalamus1
medial globus pallidus1
parietal lobe1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
CALM1295ubiquitousmarkerlateral nuclear group of thalamus, medial globus pallidus, parietal lobe

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

SymbolInteractor count
CALM125

Structural data

PDB: 1 · AlphaFold-only: 0 · No structure: 0

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
CALM1P0DP23337

Function

Pathway analysis

Distinct Reactome pathways touched by cohort: 144. Enrichment computed across 1 evidence-associated genes (1 with Reactome annotation).

Pathways by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

PathwayCohort genesFoldFDRSample cohort genes
Ionotropic activity of kainate receptors15710.0×0.006CALM1
Activation of kainate receptors upon glutamate binding15710.0×0.006CALM1
Cam-PDE 1 activation12855.0×0.006CALM1
Loss of phosphorylation of MECP2 at T30812855.0×0.006CALM1
Metabolism of nitric oxide: NOS3 activation and regulation12284.0×0.006CALM1
Metabolism of cofactors11903.3×0.006CALM1
Glycogen metabolism11903.3×0.006CALM1
CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde11427.5×0.006CALM1
Loss of function of MECP2 in Rett syndrome11427.5×0.006CALM1
Pervasive developmental disorders11427.5×0.006CALM1
Activation of RAC1 downstream of NMDARs11427.5×0.006CALM1
Disorders of Developmental Biology11427.5×0.006CALM1
Disorders of Nervous System Development11427.5×0.006CALM1
Calcineurin activates NFAT11268.9×0.006CALM1
The phototransduction cascade11268.9×0.006CALM1
CASP4 inflammasome assembly11268.9×0.006CALM1
CaMK IV-mediated phosphorylation of CREB11142.0×0.006CALM1
Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation11142.0×0.006CALM1
Activation of Ca-permeable Kainate Receptor11142.0×0.006CALM1
Sodium/Calcium exchangers11038.2×0.006CALM1
CLEC7A (Dectin-1) induces NFAT activation11038.2×0.006CALM1
Reduction of cytosolic Ca++ levels1951.7×0.006CALM1
Uptake and function of anthrax toxins1951.7×0.006CALM1
eNOS activation1878.5×0.006CALM1
CREB1 phosphorylation through the activation of Adenylate Cyclase1878.5×0.006CALM1
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling1878.5×0.006CALM1
Downstream signaling events of B Cell Receptor (BCR)1815.7×0.006CALM1
Uptake and actions of bacterial toxins1815.7×0.006CALM1
Enterobacterial factors antagonize host defense1815.7×0.006CALM1
Glycogen breakdown (glycogenolysis)1761.3×0.006CALM1

GO biological processes by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

GO termCohort genesFoldFDRSample cohort genes
negative regulation of ryanodine-sensitive calcium-release channel activity18426.0×0.001CALM1
negative regulation of high voltage-gated calcium channel activity18426.0×0.001CALM1
regulation of ryanodine-sensitive calcium-release channel activity15617.3×0.001CALM1
organelle localization by membrane tethering15617.3×0.001CALM1
negative regulation of calcium ion export across plasma membrane14213.0×0.001CALM1
presynaptic endocytosis13370.4×0.001CALM1
regulation of cardiac muscle cell action potential12808.7×0.001CALM1
autophagosome membrane docking12407.4×0.001CALM1
obsolete mitochondrion-endoplasmic reticulum membrane tethering12106.5×0.001CALM1
regulation of cell communication by electrical coupling involved in cardiac conduction11872.4×0.001CALM1
calcineurin-mediated signaling11532.0×0.002CALM1
detection of calcium ion11123.5×0.002CALM1
regulation of calcium-mediated signaling11123.5×0.002CALM1
regulation of cardiac muscle contraction1887.0×0.002CALM1
regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum1674.1×0.002CALM1
regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion1674.1×0.002CALM1
cellular response to interferon-beta1526.6×0.003CALM1
regulation of heart rate1468.1×0.003CALM1
positive regulation of receptor signaling pathway via JAK-STAT1432.1×0.003CALM1
regulation of cytokinesis1421.3×0.003CALM1
substantia nigra development1366.4×0.003CALM1
response to calcium ion1318.0×0.004CALM1
G2/M transition of mitotic cell cycle1312.1×0.004CALM1
long-term synaptic potentiation1280.9×0.004CALM1
cellular response to type II interferon1208.1×0.005CALM1
G protein-coupled receptor signaling pathway136.2×0.028CALM1

Therapeutics

Drug target analysis

Approved (phase 4): 1 · Phase ≥3: 1 · Phased (≥1): 1 · Undrugged: 0

Druggability breadth: 1 of 1 evidence-associated genes (100%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).

Genes with an approved drug

The molecule shown is one approved compound that hits the gene — not necessarily a drug of choice or one indicated for this disease.

SymbolExample approved molecule
CALM1CLOZAPINE

Top cohort targets by molecule count

SymbolMoleculesMax phase
CALM164

Drugs targeting cohort genes (top 30)

MoleculeMax phaseTargets in cohort
CLOZAPINE4CALM1
TRIFLUOPERAZINE4CALM1
PROMETHAZINE4CALM1
CHLORPROMAZINE4CALM1
HESPERIDIN3CALM1
QUERCETIN3CALM1

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 0.

Cohort genes with ChEMBL bioactivity (full, sorted by assay count)

SymbolAssaysType breakdown
CALM123Binding:23

Pharmacogenomics

Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.

No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).

Chemical tractability of cohort targets

6 approved/phased compounds have measured bioactivity against a cohort gene (and aren’t yet in disease-level trials). This is a research / tractability signal, NOT a therapeutic recommendation — a bioactivity row often reflects off-target or screening binding (e.g. promiscuous kinase inhibitors against a cohort kinase), implying no disease mechanism.

CompoundMax phaseCohort target (bioactivity)
CLOZAPINE4CALM1
TRIFLUOPERAZINE4CALM1
PROMETHAZINE4CALM1
CHLORPROMAZINE4CALM1
HESPERIDIN3CALM1
QUERCETIN3CALM1

Druggability pyramid

Cohort genes binned by druggability tier (high → low):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)1CALM1
BPhased (≥1) drug, not yet approved0
CDruggable family + PDB, no drug0
DDruggable family + AlphaFold only, no drug0
EDifficult family or no structure, no drug0

Undrugged target profiles

0 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).

Clinical trials & evidence

Clinical trials

Clinical trials: 0.