Piirre
Palpitations
A sensation that the heart is pounding or racing, which is a non-specific sign but may be a manifestation of arrhythmia.
Yhteenveto
- Tunnetaan myös nimellä
- Missed heart beat, Skipped heart beat, Heart palpitations
- Elimistön järjestelmä
- Abnormality of the cardiovascular system
ViitegenomiGRCh38hg38
Geenien ja varianttien sivujen sijainnit noudattavat tätä valintaa tässä selaimessa.
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Tilaa Genome Test107 geeniä, jotka liittyvät piirteeseen Palpitations
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Palpitations esiintyy. Useimmilla, joilla on tämä piirre, ei ole mitään näistä sairauksista, eikä tämän listan geeni kerro mitään kenenkään omasta genomista.
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| CAV3caveolin 3 | Aina | 2 sairaudessa |
| CDH2cadherin 2 | Aina | 1 sairaudessa |
| DTNAdystrobrevin alpha | Aina | 1 sairaudessa |
| EMDemerin | Aina | 2 sairaudessa |
| GCGRglucagon receptor | Aina | 1 sairaudessa |
| KCND3potassium voltage-gated channel subfamily D member 3 | Aina | 1 sairaudessa |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Aina | 3 sairaudessa |
| MYZAPmyocardial zonula adherens protein | Aina | 1 sairaudessa |
| POPDC2popeye domain cAMP effector 2 | Aina | 1 sairaudessa |
| TECRLtrans-2,3-enoyl-CoA reductase like | Aina | 1 sairaudessa |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Hyvin usein (80–99%) | 2 sairaudessa |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Hyvin usein (80–99%) | 1 sairaudessa |
| KCNA5potassium voltage-gated channel subfamily A member 5 | Hyvin usein (80–99%) | 2 sairaudessa |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Hyvin usein (80–99%) | 2 sairaudessa |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Hyvin usein (80–99%) | 1 sairaudessa |
| LAMP2lysosome associated membrane protein 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| MEN1menin 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| NPPAnatriuretic peptide A | Hyvin usein (80–99%) | 3 sairaudessa |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Hyvin usein (80–99%) | 3 sairaudessa |
| YY1YY1 transcription factor | Hyvin usein (80–99%) | 1 sairaudessa |
| ABCC8ATP binding cassette subfamily C member 8 | Usein (30–79%) | 1 sairaudessa |
| ABCC9ATP binding cassette subfamily C member 9 | Usein (30–79%) | 1 sairaudessa |
| ACTC1actin alpha cardiac muscle 1 | Usein (30–79%) | 2 sairaudessa |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Usein (30–79%) | 1 sairaudessa |
| CDH23cadherin related 23 | Usein (30–79%) | 1 sairaudessa |
| CDKN2Acyclin dependent kinase inhibitor 2A | Usein (30–79%) | 1 sairaudessa |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Usein (30–79%) | 2 sairaudessa |
| CTNNB1catenin beta 1 | Usein (30–79%) | 1 sairaudessa |
| DLSTdihydrolipoamide S-succinyltransferase | Usein (30–79%) | 1 sairaudessa |
| DNMT3ADNA methyltransferase 3 alpha | Usein (30–79%) | 1 sairaudessa |
| DSC2desmocollin 2 | Usein (30–79%) | 1 sairaudessa |
| DSG2desmoglein 2 | Usein (30–79%) | 1 sairaudessa |
| EPAS1endothelial PAS domain protein 1 | Usein (30–79%) | 1 sairaudessa |
| FHfumarate hydratase | Usein (30–79%) | 1 sairaudessa |
| GATA4GATA binding protein 4 | Usein (30–79%) | 2 sairaudessa |
| GATA5GATA binding protein 5 | Usein (30–79%) | 1 sairaudessa |
| GATA6GATA binding protein 6 | Usein (30–79%) | 2 sairaudessa |
| GJA5gap junction protein alpha 5 | Usein (30–79%) | 1 sairaudessa |
| GYG1glycogenin 1 | Usein (30–79%) | 1 sairaudessa |
| HNF1AHNF1 homeobox A | Usein (30–79%) | 1 sairaudessa |
Näytä 67 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| JPH2junctophilin 2 | Usein (30–79%) | 1 sairaudessa |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Usein (30–79%) | 1 sairaudessa |
| KCNH2potassium voltage-gated channel subfamily H member 2 | Usein (30–79%) | 2 sairaudessa |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Usein (30–79%) | 1 sairaudessa |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Usein (30–79%) | 6 sairaudessa |
| KCNJ3potassium inwardly rectifying channel subfamily J member 3 | Usein (30–79%) | 1 sairaudessa |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Usein (30–79%) | 2 sairaudessa |
| KIF1Bkinesin family member 1B | Usein (30–79%) | 1 sairaudessa |
| KLHL24kelch like family member 24 | Usein (30–79%) | 1 sairaudessa |
| MAXMYC associated transcriptional regulator X | Usein (30–79%) | 1 sairaudessa |
| MDH2malate dehydrogenase 2 | Usein (30–79%) | 1 sairaudessa |
| MYH6myosin heavy chain 6 | Usein (30–79%) | 1 sairaudessa |
| MYH7myosin heavy chain 7 | Usein (30–79%) | 1 sairaudessa |
| MYL4myosin light chain 4 | Usein (30–79%) | 2 sairaudessa |
| MYOZ2myozenin 2 | Usein (30–79%) | 1 sairaudessa |
| NF1neurofibromin 1 | Usein (30–79%) | 1 sairaudessa |
| NKX2-5NK2 homeobox 5 | Usein (30–79%) | 2 sairaudessa |
| NKX2-6NK2 homeobox 6 | Usein (30–79%) | 1 sairaudessa |
| NUP155nucleoporin 155 | Usein (30–79%) | 1 sairaudessa |
| PITX2paired like homeodomain 2 | Usein (30–79%) | 1 sairaudessa |
| PKP2plakophilin 2 | Usein (30–79%) | 1 sairaudessa |
| PNPLA2patatin like domain 2, triacylglycerol lipase | Usein (30–79%) | 1 sairaudessa |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Usein (30–79%) | 1 sairaudessa |
| RETret proto-oncogene | Usein (30–79%) | 3 sairaudessa |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Usein (30–79%) | 1 sairaudessa |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Usein (30–79%) | 1 sairaudessa |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Usein (30–79%) | 1 sairaudessa |
| SCN4Bsodium voltage-gated channel beta subunit 4 | Usein (30–79%) | 1 sairaudessa |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Usein (30–79%) | 1 sairaudessa |
| SDHAF2succinate dehydrogenase complex assembly factor 2 | Usein (30–79%) | 1 sairaudessa |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Usein (30–79%) | 3 sairaudessa |
| SDHCsuccinate dehydrogenase complex subunit C | Usein (30–79%) | 2 sairaudessa |
| SDHDsuccinate dehydrogenase complex subunit D | Usein (30–79%) | 4 sairaudessa |
| SLC25A11solute carrier family 25 member 11 | Usein (30–79%) | 1 sairaudessa |
| SLC4A3solute carrier family 4 member 3 | Usein (30–79%) | 1 sairaudessa |
| TBX20T-box transcription factor 20 | Usein (30–79%) | 1 sairaudessa |
| TERTtelomerase reverse transcriptase | Usein (30–79%) | 1 sairaudessa |
| TLL1tolloid like 1 | Usein (30–79%) | 2 sairaudessa |
| TMEM126Btransmembrane protein 126B | Usein (30–79%) | 1 sairaudessa |
| TMEM127transmembrane protein 127 | Usein (30–79%) | 1 sairaudessa |
| TP53tumor protein p53 | Usein (30–79%) | 1 sairaudessa |
| TTNtitin | Usein (30–79%) | 1 sairaudessa |
| UCP2uncoupling protein 2 | Usein (30–79%) | 1 sairaudessa |
| VHLvon Hippel-Lindau tumor suppressor | Usein (30–79%) | 3 sairaudessa |
| ZNRF3zinc and ring finger 3 | Usein (30–79%) | 1 sairaudessa |
| ADAMTS19ADAM metallopeptidase with thrombospondin type 1 motif 19 | Joskus (5–29%) | 1 sairaudessa |
| BAG3BAG cochaperone 3 | Joskus (5–29%) | 1 sairaudessa |
| CCND1cyclin D1 | Joskus (5–29%) | 1 sairaudessa |
| JUPjunction plakoglobin | Joskus (5–29%) | 1 sairaudessa |
| THRBthyroid hormone receptor beta | Joskus (5–29%) | 1 sairaudessa |
| TRIM63tripartite motif containing 63 | Joskus (5–29%) | 1 sairaudessa |
| ATRXATRX chromatin remodeler | Harvinainen (1–4 %) | 1 sairaudessa |
| CLCNKBchloride voltage-gated channel Kb | Harvinainen (1–4 %) | 1 sairaudessa |
| POLGDNA polymerase gamma, catalytic subunit | Harvinainen (1–4 %) | 1 sairaudessa |
| POLG2DNA polymerase gamma 2, accessory subunit | Harvinainen (1–4 %) | 1 sairaudessa |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Harvinainen (1–4 %) | 1 sairaudessa |
| SLC12A3solute carrier family 12 member 3 | Harvinainen (1–4 %) | 2 sairaudessa |
| SLC25A4solute carrier family 25 member 4 | Harvinainen (1–4 %) | 1 sairaudessa |
| TWNKtwinkle mtDNA helicase | Harvinainen (1–4 %) | 1 sairaudessa |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Ei kirjattu | 1 sairaudessa |
| ISCUiron-sulfur cluster assembly enzyme | Ei kirjattu | 1 sairaudessa |
| MYL2myosin light chain 2 | Ei kirjattu | 1 sairaudessa |
| MYL3myosin light chain 3 | Ei kirjattu | 1 sairaudessa |
| POPDC1popeye domain cAMP effector 1 | Ei kirjattu | 1 sairaudessa |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Ei kirjattu | 2 sairaudessa |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Ei kirjattu | 1 sairaudessa |
| TMEM43transmembrane protein 43 | Ei kirjattu | 1 sairaudessa |
Kuinka usein ilmiö esiintyy ihmisillä, joilla on jokin geenin sairauksista, niin kuin Human Phenotype Ontology sen kirjaa. Nämä sivut kuvaavat piirteitä ja niiden taustalla olevaa tutkimusta, eivätkä ne ole diagnoosi. Oireista kannattaa kysyä lääkäriltä tai geneettiseltä neuvojalta.
Laajemmat piirteet
Mistä tämä tieto tulee
- Human Phenotype Ontology, julkaisu 2026-09-01: piirre, sen nimet, määritelmä ja siihen liitetyt geenit. Lue lisää osoitteesta hpo.jax.org.
- Tietojulkaisu 2026.10.16-c6eea6bf.
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