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Egenskap
Slow heartbeats
Kliniskt namn: Bradycardia
A slower than normal heart rate (in adults, slower than 60 beats per minute).
Sammanfattning
- Även kallad
- Brachycardia
- Kroppssystem
- Abnormality of the cardiovascular system
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Lägg till .json i sidans adress, eller begär application/json, för att läsa den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/bradycardia.json"
page <- fromJSON(url)
page$trait$nameSlow heartbeatsHP:0001662
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Läs generna kopplade till Slow heartbeats, och resten av ditt genom, med ett enda test.
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Beställ mitt Genome Test54 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Long QT SyndromeReads 7 of these genesCALM3CACNA1CKCNH2KCNJ2KCNQ1SCN5AAbout this report →
- Congenital HypothyroidismReads 9 of these genesDUOX2DUOXA2IYDSLC5A5TGTPOAbout this report →
- Short Qt SyndromeReads 4 of these genesKCNH2KCNJ2KCNQ1SLC4A3About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 5 of these genesCACNA1DHCN4SCN5ADESTRPM4About this report →
Show 50 more reports
- Thyroid CancerReads 9 of these genesDUOX2DUOXA2IYDSLC5A5TGTPOAbout this report →
- Familial Atrial FibrillationReads 3 of these genesKCNJ2KCNQ1MYL4About this report →
- Surfactant Metabolism DysfunctionReads 3 of these genesABCA3SFTPBSFTPCAbout this report →
- Familial Periodic ParalysisReads 2 of these genesSCN4AKCNJ2About this report →
- Catecholaminergic Polymorphic Ventricular TachycardiaReads 3 of these genesCALM3CALM2CASQ2About this report →
- 3-Methylglutaconic Aciduria Type 8 (HTRA2)Reads 1 of these genesHTRA2About this report →
- Aminoacylase 1 DeficiencyReads 1 of these genesACY1About this report →
- BRAT1-Related Neurodevelopmental Disorder with Cerebellar AtrophyReads 1 of these genesBRAT1About this report →
- Brugada SyndromeReads 1 of these genesSCN5AAbout this report →
- ECHS1 DeficiencyReads 1 of these genesECHS1About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 5 of these genesHESX1LHX3LHX4POU1F1PROP1About this report →
- Primary Mitochondrial DiseaseReads 11 of these genesMPV17MTO1NDUFA2SCO1UQCRFS1COQ4About this report →
- Epidermolysis BullosaReads 4 of these genesDSTLAMA3LAMB3LAMC2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 12 of these genesMPV17NDUFA2COQ4DSTECHS1GFM2About this report →
- Tuberous SclerosisReads 1 of these genesTSC2About this report →
- Hypogonadotropic HypogonadismReads 5 of these genesHESX1LHX3LHX4POU1F1PROP1About this report →
- Arrhythmogenic CardiomyopathyReads 2 of these genesDESTMEM43About this report →
- Leigh SyndromeReads 5 of these genesNDUFA2ECHS1GFM2SCO2LIPT1About this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- Dilated CardiomyopathyReads 4 of these genesSCN5APPA2DESDOLKAbout this report →
- Methylmalonic & Propionic AcidemiaReads 2 of these genesMMACHCPRDX1About this report →
- Homocystinuria & Cobalamin DisordersReads 2 of these genesMMACHCPRDX1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesDSTSCN9AAbout this report →
- Renal Tubular AcidosisReads 1 of these genesSLC4A3About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesPRKAG2About this report →
- Epilepsy (Full Panel)Reads 4 of these genesBRAT1GLULGRIN1SCN9AAbout this report →
- LipodystrophyReads 1 of these genesCAVIN1About this report →
- Type I InterferonopathiesReads 1 of these genesUSP18About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesTLL1About this report →
- Myofibrillar MyopathiesReads 1 of these genesDESAbout this report →
- Glycogen Storage DiseaseReads 1 of these genesGBE1About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesCACNA1DAbout this report →
- Cutis LaxaReads 1 of these genesEFEMP2About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesSLC25A20About this report →
- Amelogenesis ImperfectaReads 1 of these genesLAMB3About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesTSPYL1About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesMPV17SCO2About this report →
- Congenital MyopathiesReads 1 of these genesACTA1About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesDHDDSDOLKAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesUSP18About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesTRPM4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSCN4AAbout this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTWNKAbout this report →
- Intellectual DisabilityReads 2 of these genesGRIN1ASXL1About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesPRKAG2About this report →
- Retinitis PigmentosaReads 1 of these genesDHDDSAbout this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesTANGO2TWNKAbout this report →
Läs generna kopplade till Slow heartbeats, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test84 gener kopplade till Slow heartbeats
Förändringar i dessa gener orsakar sällsynta tillstånd där Slow heartbeats förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| ACY1aminoacylase 1 | Alltid | I 1 tillstånd |
| BRAT1BRCA1 associated ATM activator 1 | Alltid | I 1 tillstånd |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Alltid | I 1 tillstånd |
| CALM3calmodulin 3 | Alltid | I 1 tillstånd |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Alltid | I 1 tillstånd |
| DMRT2doublesex and mab-3 related transcription factor 2 | Alltid | I 1 tillstånd |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Alltid | I 1 tillstånd |
| FAAP100FA core complex associated protein 100 | Alltid | I 1 tillstånd |
| GLULglutamate-ammonia ligase | Alltid | I 1 tillstånd |
| GNB5G protein subunit beta 5 | Alltid | I 3 tillstånd |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Alltid | I 1 tillstånd |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Alltid | I 1 tillstånd |
| MPV17mitochondrial inner membrane protein MPV17 | Alltid | I 1 tillstånd |
| MTO1mitochondrial tRNA translation optimization 1 | Alltid | I 1 tillstånd |
| NDUFA2NADH:ubiquinone oxidoreductase subunit A2 | Alltid | I 1 tillstånd |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Alltid | I 1 tillstånd |
| SCO1synthesis of cytochrome C oxidase 1 | Alltid | I 1 tillstånd |
| SGO1shugoshin 1 | Alltid | I 1 tillstånd |
| TM2D3TM2 domain containing 3 | Alltid | I 1 tillstånd |
| UQCRFS1ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 | Alltid | I 1 tillstånd |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Mycket ofta (80–99 %) | I 1 tillstånd |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| KCNH2potassium voltage-gated channel subfamily H member 2 | Mycket ofta (80–99 %) | I 1 tillstånd |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Mycket ofta (80–99 %) | I 1 tillstånd |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Mycket ofta (80–99 %) | I 2 tillstånd |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Mycket ofta (80–99 %) | I 2 tillstånd |
| SLC4A3solute carrier family 4 member 3 | Mycket ofta (80–99 %) | I 1 tillstånd |
| ASXL1ASXL transcriptional regulator 1 | Ofta (30–79 %) | I 1 tillstånd |
| CALM2calmodulin 2 | Ofta (30–79 %) | I 1 tillstånd |
| COQ4coenzyme Q4 | Ofta (30–79 %) | I 1 tillstånd |
| DSTdystonin | Ofta (30–79 %) | I 2 tillstånd |
| ECHS1enoyl-CoA hydratase, short chain 1 | Ofta (30–79 %) | I 1 tillstånd |
| GBE11,4-alpha-glucan branching enzyme 1 | Ofta (30–79 %) | I 1 tillstånd |
| GFM2GTP dependent ribosome recycling factor mitochondrial 2 | Ofta (30–79 %) | I 1 tillstånd |
| GLYCTKglycerate kinase | Ofta (30–79 %) | I 1 tillstånd |
| HESX1HESX homeobox 1 | Ofta (30–79 %) | I 1 tillstånd |
| IFNGinterferon gamma | Ofta (30–79 %) | I 1 tillstånd |
| LHX3LIM homeobox 3 | Ofta (30–79 %) | I 1 tillstånd |
| LHX4LIM homeobox 4 | Ofta (30–79 %) | I 1 tillstånd |
| MMACHCmetabolism of cobalamin associated C | Ofta (30–79 %) | I 1 tillstånd |
Visa 44 gener till
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| NDUFA8NADH:ubiquinone oxidoreductase subunit A8 | Ofta (30–79 %) | I 1 tillstånd |
| POU1F1POU class 1 homeobox 1 | Ofta (30–79 %) | I 1 tillstånd |
| PPA2inorganic pyrophosphatase 2 | Ofta (30–79 %) | I 1 tillstånd |
| PRDX1peroxiredoxin 1 | Ofta (30–79 %) | I 1 tillstånd |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Ofta (30–79 %) | I 1 tillstånd |
| PROP1PROP paired-like homeobox 1 | Ofta (30–79 %) | I 1 tillstånd |
| SCO2synthesis of cytochrome C oxidase 2 | Ofta (30–79 %) | I 1 tillstånd |
| TSC2TSC complex subunit 2 | Ofta (30–79 %) | I 1 tillstånd |
| ABCA3ATP binding cassette subfamily A member 3 | Ibland (5–29 %) | I 1 tillstånd |
| ACTA1actin alpha 1, skeletal muscle | Ibland (5–29 %) | I 1 tillstånd |
| CRELD1CRELD disulfide isomerase 1 | Ibland (5–29 %) | I 1 tillstånd |
| DESdesmin | Ibland (5–29 %) | I 1 tillstånd |
| DOLKdolichol kinase | Ibland (5–29 %) | I 1 tillstånd |
| DUOX2dual oxidase 2 | Ibland (5–29 %) | I 1 tillstånd |
| DUOXA2dual oxidase maturation factor 2 | Ibland (5–29 %) | I 1 tillstånd |
| HTRA2HtrA serine peptidase 2 | Ibland (5–29 %) | I 1 tillstånd |
| IYDiodotyrosine deiodinase | Ibland (5–29 %) | I 1 tillstånd |
| MYL4myosin light chain 4 | Ibland (5–29 %) | I 1 tillstånd |
| NFU1NFU1 iron-sulfur cluster scaffold | Ibland (5–29 %) | I 1 tillstånd |
| NPPAnatriuretic peptide A | Ibland (5–29 %) | I 2 tillstånd |
| SFTPBsurfactant protein B | Ibland (5–29 %) | I 1 tillstånd |
| SFTPCsurfactant protein C | Ibland (5–29 %) | I 1 tillstånd |
| SLC5A5solute carrier family 5 member 5 | Ibland (5–29 %) | I 1 tillstånd |
| TANGO2transport and golgi organization 2 homolog | Ibland (5–29 %) | I 1 tillstånd |
| TGthyroglobulin | Ibland (5–29 %) | I 1 tillstånd |
| TLL1tolloid like 1 | Ibland (5–29 %) | I 1 tillstånd |
| TPOthyroid peroxidase | Ibland (5–29 %) | I 1 tillstånd |
| TSHBthyroid stimulating hormone subunit beta | Ibland (5–29 %) | I 1 tillstånd |
| TSHRthyroid stimulating hormone receptor | Ibland (5–29 %) | I 1 tillstånd |
| TWNKtwinkle mtDNA helicase | Ibland (5–29 %) | I 1 tillstånd |
| USP18ubiquitin specific peptidase 18 | Ibland (5–29 %) | I 1 tillstånd |
| LAMA3laminin subunit alpha 3 | Sällan (1–4%) | I 1 tillstånd |
| LAMB3laminin subunit beta 3 | Sällan (1–4%) | I 1 tillstånd |
| LAMC2laminin subunit gamma 2 | Sällan (1–4%) | I 1 tillstånd |
| CASQ2calsequestrin 2 | Inte registrerat | I 1 tillstånd |
| CAVIN1caveolae associated protein 1 | Inte registrerat | I 1 tillstånd |
| COQ9coenzyme Q9 | Inte registrerat | I 1 tillstånd |
| LIPT1lipoyltransferase 1 | Inte registrerat | I 1 tillstånd |
| PAX8paired box 8 | Inte registrerat | I 1 tillstånd |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Inte registrerat | I 1 tillstånd |
| SLC25A20solute carrier family 25 member 20 | Inte registrerat | I 1 tillstånd |
| TMEM43transmembrane protein 43 | Inte registrerat | I 1 tillstånd |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Inte registrerat | I 1 tillstånd |
| TSPYL1TSPY like 1 | Inte registrerat | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
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Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.19-9814e911.
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Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
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