Egenskap
Chest pain
An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the chest.
Sammendrag
- Også kalt
- Thoracic pain
- Kroppssystem
- Constitutional symptom
ReferansegenomGRCh38hg38
Posisjoner på gen- og variantsidene følger dette valget i denne nettleseren.
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Få mitt Genome Test143 gener knyttet til Chest pain
Endringer i disse genene forårsaker sjeldne tilstander der Chest pain forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| EMDemerin | Alltid | I 1 tilstand |
| POPDC2popeye domain cAMP effector 2 | Alltid | I 1 tilstand |
| SOX17SRY-box transcription factor 17 | Alltid | I 1 tilstand |
| CALRcalreticulin | Svært ofte (80–99 %) | I 1 tilstand |
| JAK2Janus kinase 2 | Svært ofte (80–99 %) | I 2 tilstander |
| MPLMPL proto-oncogene, thrombopoietin receptor | Svært ofte (80–99 %) | I 2 tilstander |
| SH2B3SH2B adaptor protein 3 | Svært ofte (80–99 %) | I 1 tilstand |
| TET2tet methylcytosine dioxygenase 2 | Svært ofte (80–99 %) | I 1 tilstand |
| TP53tumor protein p53 | Svært ofte (80–99 %) | I 1 tilstand |
| TSC1TSC complex subunit 1 | Svært ofte (80–99 %) | I 1 tilstand |
| TSC2TSC complex subunit 2 | Svært ofte (80–99 %) | I 1 tilstand |
| ABCC9ATP binding cassette subfamily C member 9 | Ofte (30–79 %) | I 1 tilstand |
| ACTA2actin alpha 2, smooth muscle | Ofte (30–79 %) | I 1 tilstand |
| BAP1BRCA1 associated deubiquitinase 1 | Ofte (30–79 %) | I 1 tilstand |
| BTNL2butyrophilin like 2 | Ofte (30–79 %) | I 2 tilstander |
| CDH2cadherin 2 | Ofte (30–79 %) | I 1 tilstand |
| CFTRCF transmembrane conductance regulator | Ofte (30–79 %) | I 1 tilstand |
| COL3A1collagen type III alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COL4A5collagen type IV alpha 5 chain | Ofte (30–79 %) | I 1 tilstand |
| COL4A6collagen type IV alpha 6 chain | Ofte (30–79 %) | I 1 tilstand |
| CRLF1cytokine receptor like factor 1 | Ofte (30–79 %) | I 1 tilstand |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Ofte (30–79 %) | I 1 tilstand |
| DLEC1DLEC1 cilia and flagella associated protein | Ofte (30–79 %) | I 1 tilstand |
| DLSTdihydrolipoamide S-succinyltransferase | Ofte (30–79 %) | I 1 tilstand |
| DNMT3ADNA methyltransferase 3 alpha | Ofte (30–79 %) | I 1 tilstand |
| DPM3dolichyl-phosphate mannosyltransferase subunit 3, regulatory | Ofte (30–79 %) | I 1 tilstand |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Ofte (30–79 %) | I 1 tilstand |
| ELNelastin | Ofte (30–79 %) | I 1 tilstand |
| EPAS1endothelial PAS domain protein 1 | Ofte (30–79 %) | I 1 tilstand |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Ofte (30–79 %) | I 1 tilstand |
| FBN1fibrillin 1 | Ofte (30–79 %) | I 1 tilstand |
| FHfumarate hydratase | Ofte (30–79 %) | I 1 tilstand |
| FOXE3forkhead box E3 | Ofte (30–79 %) | I 1 tilstand |
| GATA4GATA binding protein 4 | Ofte (30–79 %) | I 1 tilstand |
| GATA5GATA binding protein 5 | Ofte (30–79 %) | I 1 tilstand |
| GATA6GATA binding protein 6 | Ofte (30–79 %) | I 1 tilstand |
| GJA5gap junction protein alpha 5 | Ofte (30–79 %) | I 1 tilstand |
| HBBhemoglobin subunit beta | Ofte (30–79 %) | I 1 tilstand |
| HEY2hes related family bHLH transcription factor with YRPW motif 2 | Ofte (30–79 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Ofte (30–79 %) | I 1 tilstand |
Vis 103 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Ofte (30–79 %) | I 1 tilstand |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Ofte (30–79 %) | I 1 tilstand |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Ofte (30–79 %) | I 1 tilstand |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Ofte (30–79 %) | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Ofte (30–79 %) | I 3 tilstander |
| IL12Binterleukin 12B | Ofte (30–79 %) | I 1 tilstand |
| KCNA5potassium voltage-gated channel subfamily A member 5 | Ofte (30–79 %) | I 1 tilstand |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Ofte (30–79 %) | I 1 tilstand |
| KCNJ3potassium inwardly rectifying channel subfamily J member 3 | Ofte (30–79 %) | I 1 tilstand |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Ofte (30–79 %) | I 1 tilstand |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Ofte (30–79 %) | I 1 tilstand |
| KIF1Bkinesin family member 1B | Ofte (30–79 %) | I 1 tilstand |
| LAMP2lysosome associated membrane protein 2 | Ofte (30–79 %) | I 1 tilstand |
| LOXlysyl oxidase | Ofte (30–79 %) | I 1 tilstand |
| MAT2Amethionine adenosyltransferase 2A | Ofte (30–79 %) | I 1 tilstand |
| MAXMYC associated transcriptional regulator X | Ofte (30–79 %) | I 1 tilstand |
| MDH2malate dehydrogenase 2 | Ofte (30–79 %) | I 1 tilstand |
| MEFVMEFV innate immunity regulator, pyrin | Ofte (30–79 %) | I 3 tilstander |
| MFAP5microfibril associated protein 5 | Ofte (30–79 %) | I 1 tilstand |
| MLXMAX dimerization protein MLX | Ofte (30–79 %) | I 1 tilstand |
| MYH11myosin heavy chain 11 | Ofte (30–79 %) | I 2 tilstander |
| MYH7myosin heavy chain 7 | Ofte (30–79 %) | I 1 tilstand |
| MYL4myosin light chain 4 | Ofte (30–79 %) | I 1 tilstand |
| MYLKmyosin light chain kinase | Ofte (30–79 %) | I 1 tilstand |
| NF1neurofibromin 1 | Ofte (30–79 %) | I 1 tilstand |
| NKX2-5NK2 homeobox 5 | Ofte (30–79 %) | I 1 tilstand |
| NKX2-6NK2 homeobox 6 | Ofte (30–79 %) | I 1 tilstand |
| NOS1nitric oxide synthase 1 | Ofte (30–79 %) | I 1 tilstand |
| NPPAnatriuretic peptide A | Ofte (30–79 %) | I 1 tilstand |
| NUP155nucleoporin 155 | Ofte (30–79 %) | I 1 tilstand |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Ofte (30–79 %) | I 1 tilstand |
| PITX2paired like homeodomain 2 | Ofte (30–79 %) | I 1 tilstand |
| PPOXprotoporphyrinogen oxidase | Ofte (30–79 %) | I 1 tilstand |
| PRKG1protein kinase cGMP-dependent 1 | Ofte (30–79 %) | I 1 tilstand |
| PRTN3proteinase 3 | Ofte (30–79 %) | I 1 tilstand |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Ofte (30–79 %) | I 1 tilstand |
| RETret proto-oncogene | Ofte (30–79 %) | I 3 tilstander |
| RNF6ring finger protein 6 | 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 |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Ofte (30–79 %) | I 3 tilstander |
| SCN4Bsodium voltage-gated channel beta subunit 4 | Ofte (30–79 %) | I 1 tilstand |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Ofte (30–79 %) | I 1 tilstand |
| SCNN1Asodium channel epithelial 1 subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| SCNN1Bsodium channel epithelial 1 subunit beta | Ofte (30–79 %) | I 1 tilstand |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Ofte (30–79 %) | I 1 tilstand |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Ofte (30–79 %) | I 1 tilstand |
| SDHAF2succinate dehydrogenase complex assembly factor 2 | Ofte (30–79 %) | I 1 tilstand |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Ofte (30–79 %) | I 2 tilstander |
| SDHCsuccinate dehydrogenase complex subunit C | Ofte (30–79 %) | I 1 tilstand |
| SDHDsuccinate dehydrogenase complex subunit D | Ofte (30–79 %) | I 2 tilstander |
| SLC25A11solute carrier family 25 member 11 | Ofte (30–79 %) | I 1 tilstand |
| SLC34A2solute carrier family 34 member 2 | Ofte (30–79 %) | I 1 tilstand |
| SMAD2SMAD family member 2 | Ofte (30–79 %) | I 1 tilstand |
| SMAD3SMAD family member 3 | Ofte (30–79 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Ofte (30–79 %) | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | Ofte (30–79 %) | I 1 tilstand |
| TGFB3transforming growth factor beta 3 | Ofte (30–79 %) | I 1 tilstand |
| TGFBR1transforming growth factor beta receptor 1 | Ofte (30–79 %) | I 1 tilstand |
| TGFBR2transforming growth factor beta receptor 2 | Ofte (30–79 %) | I 2 tilstander |
| THPOthrombopoietin | Ofte (30–79 %) | I 1 tilstand |
| THSD4thrombospondin type 1 domain containing 4 | Ofte (30–79 %) | I 1 tilstand |
| TMEM127transmembrane protein 127 | Ofte (30–79 %) | I 1 tilstand |
| TTNtitin | Ofte (30–79 %) | I 1 tilstand |
| VHLvon Hippel-Lindau tumor suppressor | Ofte (30–79 %) | I 2 tilstander |
| WWOXWW domain containing oxidoreductase | Ofte (30–79 %) | I 1 tilstand |
| ACTC1actin alpha cardiac muscle 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ADAMTS19ADAM metallopeptidase with thrombospondin type 1 motif 19 | Noen ganger (5–29 %) | I 1 tilstand |
| APCAPC regulator of Wnt signaling pathway | Noen ganger (5–29 %) | I 1 tilstand |
| CAV3caveolin 3 | Noen ganger (5–29 %) | I 1 tilstand |
| CD4CD4 molecule | Noen ganger (5–29 %) | I 1 tilstand |
| CTNNB1catenin beta 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DBHdopamine beta-hydroxylase | Noen ganger (5–29 %) | I 1 tilstand |
| DSG2desmoglein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GNASGNAS complex locus | Noen ganger (5–29 %) | I 3 tilstander |
| IRF4interferon regulatory factor 4 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Noen ganger (5–29 %) | I 1 tilstand |
| MYL2myosin light chain 2 | Noen ganger (5–29 %) | I 1 tilstand |
| NDC1NDC1 transmembrane nucleoporin | Noen ganger (5–29 %) | I 1 tilstand |
| NOD2nucleotide binding oligomerization domain containing 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Noen ganger (5–29 %) | I 1 tilstand |
| RASA1RAS p21 protein activator 1 | Noen ganger (5–29 %) | I 1 tilstand |
| STAT3signal transducer and activator of transcription 3 | Noen ganger (5–29 %) | I 1 tilstand |
| STX16syntaxin 16 | Noen ganger (5–29 %) | I 1 tilstand |
| TNFRSF1ATNF receptor superfamily member 1A | Noen ganger (5–29 %) | I 1 tilstand |
| WASWASP actin nucleation promoting factor | Noen ganger (5–29 %) | I 1 tilstand |
| EXT1exostosin glycosyltransferase 1 | Sjelden (1–4%) | I 1 tilstand |
| EXT2exostosin glycosyltransferase 2 | Sjelden (1–4%) | I 1 tilstand |
| IRAK1interleukin 1 receptor associated kinase 1 | Sjelden (1–4%) | I 1 tilstand |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Sjelden (1–4%) | I 1 tilstand |
| SPP1secreted phosphoprotein 1 | Sjelden (1–4%) | I 1 tilstand |
| STAT4signal transducer and activator of transcription 4 | Sjelden (1–4%) | I 1 tilstand |
| ENGendoglin | Ikke registrert | I 1 tilstand |
| MEF2Amyocyte enhancer factor 2A | Ikke registrert | I 1 tilstand |
| MYBPC3myosin binding protein C3 | Ikke registrert | I 1 tilstand |
| PLNphospholamban | Ikke registrert | I 1 tilstand |
| PPA2inorganic pyrophosphatase 2 | Ikke registrert | I 1 tilstand |
| TMEM43transmembrane protein 43 | Ikke registrert | I 1 tilstand |
| TNNC1troponin C1, slow skeletal and cardiac type | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
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- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
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