Træk
Heart stops beating
Klinisk navn: Cardiac arrest
An abrupt loss of heart function.
Resumé
- Kropssystem
- Abnormality of the cardiovascular system
ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
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Bestil min Genome Test78 gener knyttet til Heart stops beating
Ændringer i disse gener forårsager sjældne tilstande, hvor Heart stops beating ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| CALM1calmodulin 1 | Altid | I 2 tilstande |
| DSTdystonin | Altid | I 1 tilstand |
| GYS1glycogen synthase 1 | Altid | I 1 tilstand |
| HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4 | Altid | I 2 tilstande |
| MRPL12mitochondrial ribosomal protein L12 | Altid | I 1 tilstand |
| NDUFA2NADH:ubiquinone oxidoreductase subunit A2 | Altid | I 1 tilstand |
| NRAPnebulin related anchoring protein | Altid | I 1 tilstand |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Altid | I 1 tilstand |
| SLC25A20solute carrier family 25 member 20 | Altid | I 1 tilstand |
| SOX17SRY-box transcription factor 17 | Altid | I 1 tilstand |
| TECRLtrans-2,3-enoyl-CoA reductase like | Altid | I 1 tilstand |
| TOR1Atorsin family 1 member A | Altid | I 1 tilstand |
| TSPYL1TSPY like 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ABCC9ATP binding cassette subfamily C member 9 | Ofte (30–79 %) | I 1 tilstand |
| AGKacylglycerol kinase | Ofte (30–79 %) | I 1 tilstand |
| AKAP9A-kinase anchoring protein 9 | Ofte (30–79 %) | I 1 tilstand |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Ofte (30–79 %) | I 1 tilstand |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Ofte (30–79 %) | I 1 tilstand |
| CACNB2calcium voltage-gated channel auxiliary subunit beta 2 | Ofte (30–79 %) | I 1 tilstand |
| CALM2calmodulin 2 | Ofte (30–79 %) | I 1 tilstand |
| GPD1Lglycerol-3-phosphate dehydrogenase 1 like | Ofte (30–79 %) | I 1 tilstand |
| KCND3potassium voltage-gated channel subfamily D member 3 | Ofte (30–79 %) | I 1 tilstand |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| KCNE3potassium voltage-gated channel subfamily E regulatory subunit 3 | Ofte (30–79 %) | I 2 tilstande |
| KCNE5potassium voltage-gated channel subfamily E regulatory subunit 5 | Ofte (30–79 %) | I 1 tilstand |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Ofte (30–79 %) | I 1 tilstand |
| MMACHCmetabolism of cobalamin associated C | Ofte (30–79 %) | I 1 tilstand |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Ofte (30–79 %) | I 1 tilstand |
| PKP2plakophilin 2 | Ofte (30–79 %) | I 2 tilstande |
| POPDC2popeye domain cAMP effector 2 | Ofte (30–79 %) | I 1 tilstand |
| PRDX1peroxiredoxin 1 | Ofte (30–79 %) | I 1 tilstand |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| RANGRFRAN guanine nucleotide release factor | Ofte (30–79 %) | I 1 tilstand |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Ofte (30–79 %) | I 1 tilstand |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Ofte (30–79 %) | I 1 tilstand |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Ofte (30–79 %) | I 2 tilstande |
| SCNN1Asodium channel epithelial 1 subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Ofte (30–79 %) | I 1 tilstand |
Vis 38 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| SEMA3Asemaphorin 3A | Ofte (30–79 %) | I 1 tilstand |
| SLMAPsarcolemma associated protein | Ofte (30–79 %) | I 1 tilstand |
| TRDNtriadin | Ofte (30–79 %) | I 1 tilstand |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Ofte (30–79 %) | I 1 tilstand |
| ABCA3ATP binding cassette subfamily A member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| ACTA1actin alpha 1, skeletal muscle | Nogle gange (5–29 %) | I 1 tilstand |
| ACTC1actin alpha cardiac muscle 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ACTN2actinin alpha 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ALG10BALG10 alpha-1,2-glucosyltransferase B | Nogle gange (5–29 %) | I 1 tilstand |
| C1QBPcomplement C1q binding protein | Nogle gange (5–29 %) | I 1 tilstand |
| CAV3caveolin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| CRELD1CRELD disulfide isomerase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CRLS1cardiolipin synthase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GBA1glucosylceramidase beta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| IFT56intraflagellar transport 56 | Nogle gange (5–29 %) | I 1 tilstand |
| IPO8importin 8 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNH2potassium voltage-gated channel subfamily H member 2 | Nogle gange (5–29 %) | I 2 tilstande |
| KLHL40kelch like family member 40 | Nogle gange (5–29 %) | I 1 tilstand |
| KLHL41kelch like family member 41 | Nogle gange (5–29 %) | I 1 tilstand |
| LMOD3leiomodin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| NEBnebulin | Nogle gange (5–29 %) | I 1 tilstand |
| SFTPBsurfactant protein B | Nogle gange (5–29 %) | I 1 tilstand |
| SFTPCsurfactant protein C | Nogle gange (5–29 %) | I 1 tilstand |
| SLC19A2solute carrier family 19 member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC2A10solute carrier family 2 member 10 | Nogle gange (5–29 %) | I 1 tilstand |
| SMAD2SMAD family member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SMAD3SMAD family member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFB3transforming growth factor beta 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFBR1transforming growth factor beta receptor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFBR2transforming growth factor beta receptor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Sjældent (1–4%) | I 2 tilstande |
| TNNI3KTNNI3 interacting kinase | Sjældent (1–4%) | I 1 tilstand |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Ikke registreret | I 1 tilstand |
| MYBPC3myosin binding protein C3 | Ikke registreret | I 1 tilstand |
| MYL3myosin light chain 3 | Ikke registreret | I 1 tilstand |
| SLC4A3solute carrier family 4 member 3 | Ikke registreret | I 1 tilstand |
| TANGO2transport and golgi organization 2 homolog | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
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Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.16-c6eea6bf.
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