Egenskap
Decreased ability to exercise
Klinisk navn: Exercise intolerance
A functional motor deficit where individuals whose responses to the challenges of exercise fail to achieve levels considered normal for their age and gender.
Sammendrag
- Også kalt
- Inability to exercise, Low exercise endurance, Poor exercise tolerance
- Kroppssystem
- Constitutional symptom
ReferansegenomGRCh38hg38
Posisjoner på gen- og variantsidene følger dette valget i denne nettleseren.
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Få mitt Genome Test171 gener knyttet til Decreased ability to exercise
Endringer i disse genene forårsaker sjeldne tilstander der Decreased ability to exercise 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 |
|---|---|---|
| ATP5F1DATP synthase F1 subunit delta | Alltid | I 2 tilstander |
| COA3cytochrome c oxidase assembly factor 3 | Alltid | I 1 tilstand |
| COL13A1collagen type XIII alpha 1 chain | Alltid | I 1 tilstand |
| FARSAphenylalanyl-tRNA synthetase subunit alpha | Alltid | I 1 tilstand |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Alltid | I 1 tilstand |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Alltid | I 1 tilstand |
| GAAalpha glucosidase | Alltid | I 1 tilstand |
| GYS1glycogen synthase 1 | Alltid | I 2 tilstander |
| HSPB8heat shock protein family B (small) member 8 | Alltid | I 1 tilstand |
| ISCUiron-sulfur cluster assembly enzyme | Alltid | I 1 tilstand |
| JPH1junctophilin 1 | Alltid | I 1 tilstand |
| MIEF2mitochondrial elongation factor 2 | Alltid | I 1 tilstand |
| MLIPmuscular LMNA interacting protein | Alltid | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Alltid | I 1 tilstand |
| MSL2MSL complex subunit 2 | Alltid | I 1 tilstand |
| PACSIN3protein kinase C and casein kinase substrate in neurons 3 | Alltid | I 1 tilstand |
| PHKA1phosphorylase kinase regulatory subunit alpha 1 | Alltid | I 2 tilstander |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Alltid | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Alltid | I 5 tilstander |
| POLG2DNA polymerase gamma 2, accessory subunit | Alltid | I 2 tilstander |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Alltid | I 1 tilstand |
| SLC18A3solute carrier family 18 member A3 | Alltid | I 1 tilstand |
| SLC25A4solute carrier family 25 member 4 | Alltid | I 3 tilstander |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Alltid | I 2 tilstander |
| TMEM126Btransmembrane protein 126B | Alltid | I 1 tilstand |
| TOP3ADNA topoisomerase III alpha | Alltid | I 2 tilstander |
| TRMT5tRNA methyltransferase 5 | Alltid | I 1 tilstand |
| CCDC78coiled-coil domain containing 78 | Svært ofte (80–99 %) | I 1 tilstand |
| CPT2carnitine palmitoyltransferase 2 | Svært ofte (80–99 %) | I 2 tilstander |
| DMDdystrophin | Svært ofte (80–99 %) | I 1 tilstand |
| ENO3enolase 3 | Svært ofte (80–99 %) | I 2 tilstander |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Svært ofte (80–99 %) | I 1 tilstand |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Svært ofte (80–99 %) | I 1 tilstand |
| PYGMglycogen phosphorylase, muscle associated | Svært ofte (80–99 %) | I 2 tilstander |
| RNASEH1ribonuclease H1 | Svært ofte (80–99 %) | I 2 tilstander |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Svært ofte (80–99 %) | I 4 tilstander |
| ABCC9ATP binding cassette subfamily C member 9 | Ofte (30–79 %) | I 1 tilstand |
| ACTA1actin alpha 1, skeletal muscle | Ofte (30–79 %) | I 1 tilstand |
| ACTC1actin alpha cardiac muscle 1 | Ofte (30–79 %) | I 1 tilstand |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Ofte (30–79 %) | I 1 tilstand |
Vis 131 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| C1QBPcomplement C1q binding protein | Ofte (30–79 %) | I 1 tilstand |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Ofte (30–79 %) | I 2 tilstander |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Ofte (30–79 %) | I 2 tilstander |
| COQ8Acoenzyme Q8A | Ofte (30–79 %) | I 2 tilstander |
| DTNAdystrobrevin alpha | Ofte (30–79 %) | I 1 tilstand |
| ETFAelectron transfer flavoprotein subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| ETFBelectron transfer flavoprotein subunit beta | Ofte (30–79 %) | I 1 tilstand |
| ETFDHelectron transfer flavoprotein dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| GATA4GATA binding protein 4 | Ofte (30–79 %) | I 2 tilstander |
| GATA5GATA binding protein 5 | Ofte (30–79 %) | I 1 tilstand |
| GATA6GATA binding protein 6 | Ofte (30–79 %) | I 2 tilstander |
| GJA5gap junction protein alpha 5 | Ofte (30–79 %) | I 1 tilstand |
| GLAgalactosidase alpha | Ofte (30–79 %) | I 1 tilstand |
| GMPPBGDP-mannose pyrophosphorylase B | Ofte (30–79 %) | I 2 tilstander |
| HINT1histidine triad nucleotide binding protein 1 | Ofte (30–79 %) | I 1 tilstand |
| KBTBD13kelch repeat and BTB domain containing 13 | Ofte (30–79 %) | I 2 tilstander |
| 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 |
| KLHL41kelch like family member 41 | Ofte (30–79 %) | I 1 tilstand |
| MGME1mitochondrial genome maintenance exonuclease 1 | Ofte (30–79 %) | I 2 tilstander |
| MRPS2mitochondrial ribosomal protein S2 | Ofte (30–79 %) | I 1 tilstand |
| MT-TEmitochondrially encoded tRNA-Glu (GAA/G) | Ofte (30–79 %) | I 1 tilstand |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Ofte (30–79 %) | I 1 tilstand |
| MYH6myosin heavy chain 6 | Ofte (30–79 %) | I 1 tilstand |
| MYL4myosin light chain 4 | Ofte (30–79 %) | I 1 tilstand |
| MYPNmyopalladin | Ofte (30–79 %) | I 1 tilstand |
| NEBnebulin | Ofte (30–79 %) | I 1 tilstand |
| NKX2-5NK2 homeobox 5 | Ofte (30–79 %) | I 2 tilstander |
| NKX2-6NK2 homeobox 6 | Ofte (30–79 %) | I 1 tilstand |
| NPPAnatriuretic peptide A | Ofte (30–79 %) | I 1 tilstand |
| NUP155nucleoporin 155 | Ofte (30–79 %) | I 1 tilstand |
| OBSCNobscurin, cytoskeletal calmodulin and titin-interacting RhoGEF | Ofte (30–79 %) | I 1 tilstand |
| PFKMphosphofructokinase, muscle | Ofte (30–79 %) | I 1 tilstand |
| PGAM2phosphoglycerate mutase 2 | Ofte (30–79 %) | I 2 tilstander |
| PGM1phosphoglucomutase 1 | Ofte (30–79 %) | I 1 tilstand |
| PHKG1phosphorylase kinase catalytic subunit gamma 1 | Ofte (30–79 %) | I 1 tilstand |
| PITX2paired like homeodomain 2 | Ofte (30–79 %) | I 1 tilstand |
| POLR2ARNA polymerase II subunit A | 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 |
| 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 |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Ofte (30–79 %) | I 1 tilstand |
| TBX20T-box transcription factor 20 | Ofte (30–79 %) | I 1 tilstand |
| TLL1tolloid like 1 | Ofte (30–79 %) | I 2 tilstander |
| TPM2tropomyosin 2 | Ofte (30–79 %) | I 1 tilstand |
| TPM3tropomyosin 3 | Ofte (30–79 %) | I 1 tilstand |
| TTNtitin | Ofte (30–79 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Ofte (30–79 %) | I 3 tilstander |
| YARS2tyrosyl-tRNA synthetase 2 | Ofte (30–79 %) | I 1 tilstand |
| ABCA3ATP binding cassette subfamily A member 3 | Noen ganger (5–29 %) | I 1 tilstand |
| ACAD9acyl-CoA dehydrogenase family member 9 | Noen ganger (5–29 %) | I 1 tilstand |
| ATP11AATPase phospholipid transporting 11A | Noen ganger (5–29 %) | I 1 tilstand |
| ATP5F1AATP synthase F1 subunit alpha | Noen ganger (5–29 %) | I 1 tilstand |
| ATP5F1EATP synthase F1 subunit epsilon | Noen ganger (5–29 %) | I 1 tilstand |
| ATP5MKATP synthase membrane subunit k | Noen ganger (5–29 %) | I 1 tilstand |
| ATP5POATP synthase peripheral stalk subunit OSCP | Noen ganger (5–29 %) | I 1 tilstand |
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| COL12A1collagen type XII alpha 1 chain | Noen ganger (5–29 %) | I 1 tilstand |
| DOT1LDOT1 like histone lysine methyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| DPP9dipeptidyl peptidase 9 | Noen ganger (5–29 %) | I 1 tilstand |
| DSPdesmoplakin | Noen ganger (5–29 %) | I 1 tilstand |
| EPB41erythrocyte membrane protein band 4.1 | Noen ganger (5–29 %) | I 1 tilstand |
| FAM13Afamily with sequence similarity 13 member A | Noen ganger (5–29 %) | I 1 tilstand |
| GCDHglutaryl-CoA dehydrogenase | Noen ganger (5–29 %) | I 1 tilstand |
| GYPCglycophorin C (Gerbich blood group) | Noen ganger (5–29 %) | I 1 tilstand |
| HIVEP2HIVEP zinc finger 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Noen ganger (5–29 %) | I 2 tilstander |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CYBmitochondrially encoded cytochrome b | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Noen ganger (5–29 %) | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Noen ganger (5–29 %) | I 2 tilstander |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Noen ganger (5–29 %) | I 2 tilstander |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Noen ganger (5–29 %) | I 1 tilstand |
| MUC5Bmucin 5B, oligomeric mucus/gel-forming | Noen ganger (5–29 %) | I 1 tilstand |
| PARNpoly(A)-specific ribonuclease | Noen ganger (5–29 %) | I 1 tilstand |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PHKBphosphorylase kinase regulatory subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PTPMT1protein tyrosine phosphatase mitochondrial 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RRM1ribonucleotide reductase catalytic subunit M1 | Noen ganger (5–29 %) | I 1 tilstand |
| RTEL1regulator of telomere elongation helicase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SFTPA1surfactant protein A1 | Noen ganger (5–29 %) | I 1 tilstand |
| SFTPA2surfactant protein A2 | Noen ganger (5–29 %) | I 1 tilstand |
| SFTPCsurfactant protein C | Noen ganger (5–29 %) | I 1 tilstand |
| SPTA1spectrin alpha, erythrocytic 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SPTBspectrin beta, erythrocytic | Noen ganger (5–29 %) | I 1 tilstand |
| STN1STN1 subunit of CST complex | Noen ganger (5–29 %) | I 1 tilstand |
| TERCtelomerase RNA component | Noen ganger (5–29 %) | I 1 tilstand |
| TERTtelomerase reverse transcriptase | Noen ganger (5–29 %) | I 1 tilstand |
| TK2thymidine kinase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| AGKacylglycerol kinase | Ikke registrert | I 1 tilstand |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Ikke registrert | I 1 tilstand |
| CAVIN1caveolae associated protein 1 | Ikke registrert | I 1 tilstand |
| COX10cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 | Ikke registrert | I 1 tilstand |
| COX15cytochrome c oxidase assembly factor COX15 | Ikke registrert | I 1 tilstand |
| COX6B1cytochrome c oxidase subunit 6B1 | Ikke registrert | I 1 tilstand |
| DNA2DNA replication helicase/nuclease 2 | Ikke registrert | I 1 tilstand |
| FASTKD2FASTK mitochondrial RNA regulator 2 | Ikke registrert | I 1 tilstand |
| FLAD1flavin adenine dinucleotide synthetase 1 | Ikke registrert | I 1 tilstand |
| LAMP2lysosome associated membrane protein 2 | Ikke registrert | I 1 tilstand |
| LDHAlactate dehydrogenase A | Ikke registrert | I 1 tilstand |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Ikke registrert | I 1 tilstand |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Ikke registrert | I 1 tilstand |
| PGK1phosphoglycerate kinase 1 | Ikke registrert | I 1 tilstand |
| PNPLA2patatin like domain 2, triacylglycerol lipase | Ikke registrert | I 1 tilstand |
| POPDC1popeye domain cAMP effector 1 | Ikke registrert | I 1 tilstand |
| RSPH4Aradial spoke head component 4A | Ikke registrert | I 1 tilstand |
| RSPH9radial spoke head component 9 | Ikke registrert | I 1 tilstand |
| SCO1synthesis of cytochrome C oxidase 1 | Ikke registrert | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Ikke registrert | I 1 tilstand |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Ikke registrert | I 1 tilstand |
| SLC25A32solute carrier family 25 member 32 | Ikke registrert | I 1 tilstand |
| SURF1SURF1 cytochrome c oxidase assembly factor | Ikke registrert | I 1 tilstand |
| TACO1translational activator of cytochrome c oxidase I | 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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Slik er informasjonen samlet
- 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.
- Datautgave 2026.10.16-c6eea6bf.
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Fra 449 $Gratis frakt · Resultater på 6–8 uker