Tunnus
Resting tremor
A resting tremor occurs when muscles are at rest and becomes less noticeable or disappears when the affected muscles are moved. Resting tremors are often slow and coarse.
Kokkuvõte
- Teised nimetused
- Tremor at rest, Rest tremor
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Resting tremor, and the rest of your genome, with one test.
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Telli oma Genome Test61 geeni on seotud tunnusega Resting tremor
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Resting tremor. 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 |
|---|---|---|
| ATP6AP2ATPase H+ transporting accessory protein 2 | Alati | Esineb 2 haiguses |
| EPG5ectopic P-granules 5 autophagy tethering factor | Alati | Esineb 1 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| MECP2methyl-CpG binding protein 2 | Alati | Esineb 2 haiguses |
| VPS13Cvacuolar protein sorting 13 homolog C | Alati | Esineb 1 haiguses |
| CHCHD2coiled-coil-helix-coiled-coil-helix domain containing 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PODXLpodocalyxin like | Väga sageli (80–99%) | Esineb 1 haiguses |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RAB39BRAB39B, member RAS oncogene family | Väga sageli (80–99%) | Esineb 1 haiguses |
| SYNJ1synaptojanin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ADCY5adenylate cyclase 5 | Sageli (30–79%) | Esineb 2 haiguses |
| COQ2coenzyme Q2, polyprenyltransferase | Sageli (30–79%) | Esineb 2 haiguses |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Sageli (30–79%) | Esineb 1 haiguses |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Sageli (30–79%) | Esineb 2 haiguses |
| FBXO7F-box protein 7 | Sageli (30–79%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Sageli (30–79%) | Esineb 2 haiguses |
| GIGYF2GRB10 interacting GYF protein 2 | Sageli (30–79%) | Esineb 2 haiguses |
| LRRK2leucine rich repeat kinase 2 | Sageli (30–79%) | Esineb 2 haiguses |
| MICU1mitochondrial calcium uptake 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Sageli (30–79%) | Esineb 2 haiguses |
| PLA2G6phospholipase A2 group VI | Sageli (30–79%) | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Sageli (30–79%) | Esineb 2 haiguses |
| POLG2DNA polymerase gamma 2, accessory subunit | Sageli (30–79%) | Esineb 1 haiguses |
| PRKNparkin RBR E3 ubiquitin protein ligase | Sageli (30–79%) | Esineb 1 haiguses |
| PSAPprosaposin | Sageli (30–79%) | Esineb 1 haiguses |
| PTPAprotein phosphatase 2 phosphatase activator | Sageli (30–79%) | Esineb 1 haiguses |
| RAB32RAB32, member RAS oncogene family | Sageli (30–79%) | Esineb 1 haiguses |
| RAB3ARAB3A, member RAS oncogene family | Sageli (30–79%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sageli (30–79%) | Esineb 1 haiguses |
| SLC25A4solute carrier family 25 member 4 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC9A6solute carrier family 9 member A6 | Sageli (30–79%) | Esineb 1 haiguses |
| SNCAsynuclein alpha | Sageli (30–79%) | Esineb 2 haiguses |
| TAF1TATA-box binding protein associated factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TWNKtwinkle mtDNA helicase | Sageli (30–79%) | Esineb 1 haiguses |
| UQCRC1ubiquinol-cytochrome c reductase core protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| VPS35VPS35 retromer complex component | Sageli (30–79%) | Esineb 2 haiguses |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP13A2ATPase cation transporting 13A2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 21 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNMT1DNA methyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GCH1GTP cyclohydrolase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| OPA3outer mitochondrial membrane lipid metabolism regulator OPA3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PARK7Parkinsonism associated deglycase | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTC19tetratricopeptide repeat domain 19 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VPS13Avacuolar protein sorting 13 homolog A | Mõnikord (5–29%) | Esineb 1 haiguses |
| FTLferritin light chain | Harva (1–4%) | Esineb 1 haiguses |
| MAN1B1mannosidase alpha class 1B member 1 | Harva (1–4%) | Esineb 1 haiguses |
| ADH1Calcohol dehydrogenase 1C (class I), gamma polypeptide | Pole registreeritud | Esineb 1 haiguses |
| ATXN2ataxin 2 | Pole registreeritud | Esineb 1 haiguses |
| ATXN3ataxin 3 | Pole registreeritud | Esineb 1 haiguses |
| ATXN8OSATXN8 opposite strand lncRNA | Pole registreeritud | Esineb 1 haiguses |
| FMR1fragile X messenger ribonucleoprotein 1 | Pole registreeritud | Esineb 1 haiguses |
| MAPTmicrotubule associated protein tau | Pole registreeritud | Esineb 1 haiguses |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | Pole registreeritud | Esineb 1 haiguses |
| PINK1PTEN induced kinase 1 | Pole registreeritud | Esineb 1 haiguses |
| SNCAIPsynuclein alpha interacting protein | Pole registreeritud | Esineb 1 haiguses |
| TBPTATA-box binding protein | 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.
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast