Tunnus
Slow heartbeats
Kliiniline nimetus: Bradycardia
A slower than normal heart rate (in adults, slower than 60 beats per minute).
Kokkuvõte
- Teised nimetused
- Brachycardia
- Kehasüsteem
- Abnormality of the cardiovascular system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Slow heartbeats, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test84 geeni on seotud tunnusega Slow heartbeats
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Slow heartbeats. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ACY1aminoacylase 1 | Alati | Esineb 1 haiguses |
| BRAT1BRCA1 associated ATM activator 1 | Alati | Esineb 1 haiguses |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Alati | Esineb 1 haiguses |
| CALM3calmodulin 3 | Alati | Esineb 1 haiguses |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Alati | Esineb 1 haiguses |
| DMRT2doublesex and mab-3 related transcription factor 2 | Alati | Esineb 1 haiguses |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Alati | Esineb 1 haiguses |
| FAAP100FA core complex associated protein 100 | Alati | Esineb 1 haiguses |
| GLULglutamate-ammonia ligase | Alati | Esineb 1 haiguses |
| GNB5G protein subunit beta 5 | Alati | Esineb 3 haiguses |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Alati | Esineb 1 haiguses |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Alati | Esineb 1 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Alati | Esineb 1 haiguses |
| MTO1mitochondrial tRNA translation optimization 1 | Alati | Esineb 1 haiguses |
| NDUFA2NADH:ubiquinone oxidoreductase subunit A2 | Alati | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Alati | Esineb 1 haiguses |
| SCO1synthesis of cytochrome C oxidase 1 | Alati | Esineb 1 haiguses |
| SGO1shugoshin 1 | Alati | Esineb 1 haiguses |
| TM2D3TM2 domain containing 3 | Alati | Esineb 1 haiguses |
| UQCRFS1ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 | Alati | Esineb 1 haiguses |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Väga sageli (80–99%) | Esineb 1 haiguses |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNH2potassium voltage-gated channel subfamily H member 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLC4A3solute carrier family 4 member 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ASXL1ASXL transcriptional regulator 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CALM2calmodulin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| COQ4coenzyme Q4 | Sageli (30–79%) | Esineb 1 haiguses |
| DSTdystonin | Sageli (30–79%) | Esineb 2 haiguses |
| ECHS1enoyl-CoA hydratase, short chain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GBE11,4-alpha-glucan branching enzyme 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GFM2GTP dependent ribosome recycling factor mitochondrial 2 | Sageli (30–79%) | Esineb 1 haiguses |
| GLYCTKglycerate kinase | Sageli (30–79%) | Esineb 1 haiguses |
| HESX1HESX homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| IFNGinterferon gamma | Sageli (30–79%) | Esineb 1 haiguses |
| LHX3LIM homeobox 3 | Sageli (30–79%) | Esineb 1 haiguses |
| LHX4LIM homeobox 4 | Sageli (30–79%) | Esineb 1 haiguses |
| MMACHCmetabolism of cobalamin associated C | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 44 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| NDUFA8NADH:ubiquinone oxidoreductase subunit A8 | Sageli (30–79%) | Esineb 1 haiguses |
| POU1F1POU class 1 homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PPA2inorganic pyrophosphatase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PRDX1peroxiredoxin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PROP1PROP paired-like homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SCO2synthesis of cytochrome C oxidase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TSC2TSC complex subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ABCA3ATP binding cassette subfamily A member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACTA1actin alpha 1, skeletal muscle | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRELD1CRELD disulfide isomerase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DESdesmin | Mõnikord (5–29%) | Esineb 1 haiguses |
| DOLKdolichol kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| DUOX2dual oxidase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DUOXA2dual oxidase maturation factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HTRA2HtrA serine peptidase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IYDiodotyrosine deiodinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| MYL4myosin light chain 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NFU1NFU1 iron-sulfur cluster scaffold | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPPAnatriuretic peptide A | Mõnikord (5–29%) | Esineb 2 haiguses |
| SFTPBsurfactant protein B | Mõnikord (5–29%) | Esineb 1 haiguses |
| SFTPCsurfactant protein C | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC5A5solute carrier family 5 member 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TANGO2transport and golgi organization 2 homolog | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGthyroglobulin | Mõnikord (5–29%) | Esineb 1 haiguses |
| TLL1tolloid like 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TPOthyroid peroxidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| TSHBthyroid stimulating hormone subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| TSHRthyroid stimulating hormone receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| TWNKtwinkle mtDNA helicase | Mõnikord (5–29%) | Esineb 1 haiguses |
| USP18ubiquitin specific peptidase 18 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LAMA3laminin subunit alpha 3 | Harva (1–4%) | Esineb 1 haiguses |
| LAMB3laminin subunit beta 3 | Harva (1–4%) | Esineb 1 haiguses |
| LAMC2laminin subunit gamma 2 | Harva (1–4%) | Esineb 1 haiguses |
| CASQ2calsequestrin 2 | Pole registreeritud | Esineb 1 haiguses |
| CAVIN1caveolae associated protein 1 | Pole registreeritud | Esineb 1 haiguses |
| COQ9coenzyme Q9 | Pole registreeritud | Esineb 1 haiguses |
| LIPT1lipoyltransferase 1 | Pole registreeritud | Esineb 1 haiguses |
| PAX8paired box 8 | Pole registreeritud | Esineb 1 haiguses |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Pole registreeritud | Esineb 1 haiguses |
| SLC25A20solute carrier family 25 member 20 | Pole registreeritud | Esineb 1 haiguses |
| TMEM43transmembrane protein 43 | Pole registreeritud | Esineb 1 haiguses |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Pole registreeritud | Esineb 1 haiguses |
| TSPYL1TSPY like 1 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.16-c6eea6bf.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast