Tunnus
Decreased ability to exercise
Kliiniline nimetus: 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.
Kokkuvõte
- Teised nimetused
- Inability to exercise, Low exercise endurance, Poor exercise tolerance
- Kehasüsteem
- Constitutional symptom
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Decreased ability to exercise, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test171 geeni on seotud tunnusega Decreased ability to exercise
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Decreased ability to exercise. 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 |
|---|---|---|
| ATP5F1DATP synthase F1 subunit delta | Alati | Esineb 2 haiguses |
| COA3cytochrome c oxidase assembly factor 3 | Alati | Esineb 1 haiguses |
| COL13A1collagen type XIII alpha 1 chain | Alati | Esineb 1 haiguses |
| FARSAphenylalanyl-tRNA synthetase subunit alpha | Alati | Esineb 1 haiguses |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Alati | Esineb 1 haiguses |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Alati | Esineb 1 haiguses |
| GAAalpha glucosidase | Alati | Esineb 1 haiguses |
| GYS1glycogen synthase 1 | Alati | Esineb 2 haiguses |
| HSPB8heat shock protein family B (small) member 8 | Alati | Esineb 1 haiguses |
| ISCUiron-sulfur cluster assembly enzyme | Alati | Esineb 1 haiguses |
| JPH1junctophilin 1 | Alati | Esineb 1 haiguses |
| MIEF2mitochondrial elongation factor 2 | Alati | Esineb 1 haiguses |
| MLIPmuscular LMNA interacting protein | Alati | Esineb 1 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Alati | Esineb 1 haiguses |
| MSL2MSL complex subunit 2 | Alati | Esineb 1 haiguses |
| PACSIN3protein kinase C and casein kinase substrate in neurons 3 | Alati | Esineb 1 haiguses |
| PHKA1phosphorylase kinase regulatory subunit alpha 1 | Alati | Esineb 2 haiguses |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Alati | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Alati | Esineb 5 haiguses |
| POLG2DNA polymerase gamma 2, accessory subunit | Alati | Esineb 2 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Alati | Esineb 1 haiguses |
| SLC18A3solute carrier family 18 member A3 | Alati | Esineb 1 haiguses |
| SLC25A4solute carrier family 25 member 4 | Alati | Esineb 3 haiguses |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Alati | Esineb 2 haiguses |
| TMEM126Btransmembrane protein 126B | Alati | Esineb 1 haiguses |
| TOP3ADNA topoisomerase III alpha | Alati | Esineb 2 haiguses |
| TRMT5tRNA methyltransferase 5 | Alati | Esineb 1 haiguses |
| CCDC78coiled-coil domain containing 78 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CPT2carnitine palmitoyltransferase 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| DMDdystrophin | Väga sageli (80–99%) | Esineb 1 haiguses |
| ENO3enolase 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| PYGMglycogen phosphorylase, muscle associated | Väga sageli (80–99%) | Esineb 2 haiguses |
| RNASEH1ribonuclease H1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Väga sageli (80–99%) | Esineb 4 haiguses |
| ABCC9ATP binding cassette subfamily C member 9 | Sageli (30–79%) | Esineb 1 haiguses |
| ACTA1actin alpha 1, skeletal muscle | Sageli (30–79%) | Esineb 1 haiguses |
| ACTC1actin alpha cardiac muscle 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 131 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| C1QBPcomplement C1q binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Sageli (30–79%) | Esineb 2 haiguses |
| CITED2Cbp/p300 interacting transactivator with ED-rich tail 2 | Sageli (30–79%) | Esineb 2 haiguses |
| COQ8Acoenzyme Q8A | Sageli (30–79%) | Esineb 2 haiguses |
| DTNAdystrobrevin alpha | Sageli (30–79%) | Esineb 1 haiguses |
| ETFAelectron transfer flavoprotein subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| ETFBelectron transfer flavoprotein subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| ETFDHelectron transfer flavoprotein dehydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| GATA4GATA binding protein 4 | Sageli (30–79%) | Esineb 2 haiguses |
| GATA5GATA binding protein 5 | Sageli (30–79%) | Esineb 1 haiguses |
| GATA6GATA binding protein 6 | Sageli (30–79%) | Esineb 2 haiguses |
| GJA5gap junction protein alpha 5 | Sageli (30–79%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Sageli (30–79%) | Esineb 1 haiguses |
| GMPPBGDP-mannose pyrophosphorylase B | Sageli (30–79%) | Esineb 2 haiguses |
| HINT1histidine triad nucleotide binding protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KBTBD13kelch repeat and BTB domain containing 13 | Sageli (30–79%) | Esineb 2 haiguses |
| KCNA5potassium voltage-gated channel subfamily A member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNJ3potassium inwardly rectifying channel subfamily J member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KLHL41kelch like family member 41 | Sageli (30–79%) | Esineb 1 haiguses |
| MGME1mitochondrial genome maintenance exonuclease 1 | Sageli (30–79%) | Esineb 2 haiguses |
| MRPS2mitochondrial ribosomal protein S2 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TEmitochondrially encoded tRNA-Glu (GAA/G) | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Sageli (30–79%) | Esineb 1 haiguses |
| MYH6myosin heavy chain 6 | Sageli (30–79%) | Esineb 1 haiguses |
| MYL4myosin light chain 4 | Sageli (30–79%) | Esineb 1 haiguses |
| MYPNmyopalladin | Sageli (30–79%) | Esineb 1 haiguses |
| NEBnebulin | Sageli (30–79%) | Esineb 1 haiguses |
| NKX2-5NK2 homeobox 5 | Sageli (30–79%) | Esineb 2 haiguses |
| NKX2-6NK2 homeobox 6 | Sageli (30–79%) | Esineb 1 haiguses |
| NPPAnatriuretic peptide A | Sageli (30–79%) | Esineb 1 haiguses |
| NUP155nucleoporin 155 | Sageli (30–79%) | Esineb 1 haiguses |
| OBSCNobscurin, cytoskeletal calmodulin and titin-interacting RhoGEF | Sageli (30–79%) | Esineb 1 haiguses |
| PFKMphosphofructokinase, muscle | Sageli (30–79%) | Esineb 1 haiguses |
| PGAM2phosphoglycerate mutase 2 | Sageli (30–79%) | Esineb 2 haiguses |
| PGM1phosphoglucomutase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PHKG1phosphorylase kinase catalytic subunit gamma 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PITX2paired like homeodomain 2 | Sageli (30–79%) | Esineb 1 haiguses |
| POLR2ARNA polymerase II subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN4Bsodium voltage-gated channel beta subunit 4 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Sageli (30–79%) | Esineb 1 haiguses |
| TBX20T-box transcription factor 20 | Sageli (30–79%) | Esineb 1 haiguses |
| TLL1tolloid like 1 | Sageli (30–79%) | Esineb 2 haiguses |
| TPM2tropomyosin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TPM3tropomyosin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TTNtitin | Sageli (30–79%) | Esineb 1 haiguses |
| TWNKtwinkle mtDNA helicase | Sageli (30–79%) | Esineb 3 haiguses |
| YARS2tyrosyl-tRNA synthetase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ABCA3ATP binding cassette subfamily A member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACAD9acyl-CoA dehydrogenase family member 9 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP11AATPase phospholipid transporting 11A | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5F1AATP synthase F1 subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5F1EATP synthase F1 subunit epsilon | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5MKATP synthase membrane subunit k | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5POATP synthase peripheral stalk subunit OSCP | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL12A1collagen type XII alpha 1 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| DOT1LDOT1 like histone lysine methyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| DPP9dipeptidyl peptidase 9 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DSPdesmoplakin | Mõnikord (5–29%) | Esineb 1 haiguses |
| EPB41erythrocyte membrane protein band 4.1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FAM13Afamily with sequence similarity 13 member A | Mõnikord (5–29%) | Esineb 1 haiguses |
| GCDHglutaryl-CoA dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| GYPCglycophorin C (Gerbich blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| HIVEP2HIVEP zinc finger 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CYBmitochondrially encoded cytochrome b | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MUC5Bmucin 5B, oligomeric mucus/gel-forming | Mõnikord (5–29%) | Esineb 1 haiguses |
| PARNpoly(A)-specific ribonuclease | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHKBphosphorylase kinase regulatory subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPMT1protein tyrosine phosphatase mitochondrial 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RRM1ribonucleotide reductase catalytic subunit M1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RTEL1regulator of telomere elongation helicase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SFTPA1surfactant protein A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SFTPA2surfactant protein A2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SFTPCsurfactant protein C | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTA1spectrin alpha, erythrocytic 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTBspectrin beta, erythrocytic | Mõnikord (5–29%) | Esineb 1 haiguses |
| STN1STN1 subunit of CST complex | Mõnikord (5–29%) | Esineb 1 haiguses |
| TERCtelomerase RNA component | Mõnikord (5–29%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Mõnikord (5–29%) | Esineb 1 haiguses |
| TK2thymidine kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| AGKacylglycerol kinase | Pole registreeritud | Esineb 1 haiguses |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Pole registreeritud | Esineb 1 haiguses |
| CAVIN1caveolae associated protein 1 | Pole registreeritud | Esineb 1 haiguses |
| COX10cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 | Pole registreeritud | Esineb 1 haiguses |
| COX15cytochrome c oxidase assembly factor COX15 | Pole registreeritud | Esineb 1 haiguses |
| COX6B1cytochrome c oxidase subunit 6B1 | Pole registreeritud | Esineb 1 haiguses |
| DNA2DNA replication helicase/nuclease 2 | Pole registreeritud | Esineb 1 haiguses |
| FASTKD2FASTK mitochondrial RNA regulator 2 | Pole registreeritud | Esineb 1 haiguses |
| FLAD1flavin adenine dinucleotide synthetase 1 | Pole registreeritud | Esineb 1 haiguses |
| LAMP2lysosome associated membrane protein 2 | Pole registreeritud | Esineb 1 haiguses |
| LDHAlactate dehydrogenase A | Pole registreeritud | Esineb 1 haiguses |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Pole registreeritud | Esineb 1 haiguses |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Pole registreeritud | Esineb 1 haiguses |
| PGK1phosphoglycerate kinase 1 | Pole registreeritud | Esineb 1 haiguses |
| PNPLA2patatin like domain 2, triacylglycerol lipase | Pole registreeritud | Esineb 1 haiguses |
| POPDC1popeye domain cAMP effector 1 | Pole registreeritud | Esineb 1 haiguses |
| RSPH4Aradial spoke head component 4A | Pole registreeritud | Esineb 1 haiguses |
| RSPH9radial spoke head component 9 | Pole registreeritud | Esineb 1 haiguses |
| SCO1synthesis of cytochrome C oxidase 1 | Pole registreeritud | Esineb 1 haiguses |
| SCO2synthesis of cytochrome C oxidase 2 | Pole registreeritud | Esineb 1 haiguses |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Pole registreeritud | Esineb 1 haiguses |
| SLC25A32solute carrier family 25 member 32 | Pole registreeritud | Esineb 1 haiguses |
| SURF1SURF1 cytochrome c oxidase assembly factor | Pole registreeritud | Esineb 1 haiguses |
| TACO1translational activator of cytochrome c oxidase I | 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