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Piirre
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.
Yhteenveto
- Tunnetaan myös nimellä
- Tremor at rest, Rest tremor
- Elimistön järjestelmä
- Abnormality of the nervous system
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Tämä sivu datana
Lisää sivun osoitteen perään .json tai pyydä application/json-muotoa, niin saat sivun JSON-muodossa.
library(jsonlite)
url <- "https://dantelabs.com/traits/resting-tremor.json"
page <- fromJSON(url)
page$trait$nameResting tremorHP:0002322
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Lue Resting tremor-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
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Tilaa Genome Test38 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Parkinson DiseaseReads 15 of these genesVPS13CCHCHD2DNAJC6SYNJ1FBXO7GBA1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 6 of these genesATP1A3CACNA1GDNMT1ATXN2ATXN3TBPAbout this report →
- ADCY5-Related DyskinesiaReads 1 of these genesADCY5About this report →
- Cerebrotendinous XanthomatosisReads 1 of these genesCYP27A1About this report →
Show 34 more reports
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
- DNMT1-Related Ataxia, Deafness and Narcolepsy (ADCA-DN)Reads 1 of these genesDNMT1About this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- GTP Cyclohydrolase 1 DeficiencyReads 1 of these genesGCH1About this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Vici SyndromeReads 1 of these genesEPG5About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 3 of these genesPLA2G6ATP13A2FTLAbout this report →
- Inherited Neurodegenerative DisordersReads 18 of these genesPLA2G6POLGPSAPTWNKALDH18A1ATP13A2About this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A4About this report →
- Metachromatic LeukodystrophyReads 1 of these genesPSAPAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 4 of these genesNR4A2TAF1ATP1A3GCH1About this report →
- Primary Mitochondrial DiseaseReads 7 of these genesCOQ2POLGPOLG2RRM2BSLC25A4TWNKAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 9 of these genesCOQ2PLA2G6POLGPSAPRRM2BCYP27A1About this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 1 of these genesVPS13AAbout this report →
- Hereditary Optic NeuropathyReads 2 of these genesATP1A3OPA3About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesSLC25A4About this report →
- Lysosomal Storage DiseaseReads 3 of these genesGBA1PSAPCYP27A1About this report →
- Intellectual DisabilityReads 5 of these genesATP6AP2MECP2RAB39BTAF1MAN1B1About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesGCH1About this report →
- Epilepsy (Full Panel)Reads 4 of these genesATP6AP2MECP2SYNJ1ATP1A3About this report →
- Frontotemporal DementiaReads 1 of these genesMAPTAbout this report →
- Female InfertilityReads 2 of these genesTWNKFMR1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesTWNKCYP27A1About this report →
- Cutis LaxaReads 1 of these genesALDH18A1About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesALDH18A1ATP13A2About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesPSAPCYP27A1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesDNMT1About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesFTLAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesATP6AP2MAN1B1About this report →
- Nephrotic SyndromeReads 1 of these genesPODXLAbout this report →
- Leigh SyndromeReads 1 of these genesTTC19About this report →
Lue Resting tremor-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test61 geeniä, jotka liittyvät piirteeseen Resting tremor
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Resting tremor esiintyy. Useimmilla, joilla on tämä piirre, ei ole mitään näistä sairauksista, eikä tämän listan geeni kerro mitään kenenkään omasta genomista.
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| ATP6AP2ATPase H+ transporting accessory protein 2 | Aina | 2 sairaudessa |
| EPG5ectopic P-granules 5 autophagy tethering factor | Aina | 1 sairaudessa |
| LRRC7leucine rich repeat containing 7 | Aina | 1 sairaudessa |
| MECP2methyl-CpG binding protein 2 | Aina | 2 sairaudessa |
| VPS13Cvacuolar protein sorting 13 homolog C | Aina | 1 sairaudessa |
| CHCHD2coiled-coil-helix-coiled-coil-helix domain containing 2 | Hyvin usein (80–99%) | 1 sairaudessa |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Hyvin usein (80–99%) | 1 sairaudessa |
| PODXLpodocalyxin like | Hyvin usein (80–99%) | 1 sairaudessa |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| RAB39BRAB39B, member RAS oncogene family | Hyvin usein (80–99%) | 1 sairaudessa |
| SYNJ1synaptojanin 1 | Hyvin usein (80–99%) | 1 sairaudessa |
| ADCY5adenylate cyclase 5 | Usein (30–79%) | 2 sairaudessa |
| COQ2coenzyme Q2, polyprenyltransferase | Usein (30–79%) | 2 sairaudessa |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Usein (30–79%) | 1 sairaudessa |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Usein (30–79%) | 2 sairaudessa |
| FBXO7F-box protein 7 | Usein (30–79%) | 1 sairaudessa |
| GBA1glucosylceramidase beta 1 | Usein (30–79%) | 2 sairaudessa |
| GIGYF2GRB10 interacting GYF protein 2 | Usein (30–79%) | 2 sairaudessa |
| LRRK2leucine rich repeat kinase 2 | Usein (30–79%) | 2 sairaudessa |
| MICU1mitochondrial calcium uptake 1 | Usein (30–79%) | 1 sairaudessa |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Usein (30–79%) | 2 sairaudessa |
| PLA2G6phospholipase A2 group VI | Usein (30–79%) | 1 sairaudessa |
| POLGDNA polymerase gamma, catalytic subunit | Usein (30–79%) | 2 sairaudessa |
| POLG2DNA polymerase gamma 2, accessory subunit | Usein (30–79%) | 1 sairaudessa |
| PRKNparkin RBR E3 ubiquitin protein ligase | Usein (30–79%) | 1 sairaudessa |
| PSAPprosaposin | Usein (30–79%) | 1 sairaudessa |
| PTPAprotein phosphatase 2 phosphatase activator | Usein (30–79%) | 1 sairaudessa |
| RAB32RAB32, member RAS oncogene family | Usein (30–79%) | 1 sairaudessa |
| RAB3ARAB3A, member RAS oncogene family | Usein (30–79%) | 1 sairaudessa |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Usein (30–79%) | 1 sairaudessa |
| SLC25A4solute carrier family 25 member 4 | Usein (30–79%) | 1 sairaudessa |
| SLC9A6solute carrier family 9 member A6 | Usein (30–79%) | 1 sairaudessa |
| SNCAsynuclein alpha | Usein (30–79%) | 2 sairaudessa |
| TAF1TATA-box binding protein associated factor 1 | Usein (30–79%) | 1 sairaudessa |
| TWNKtwinkle mtDNA helicase | Usein (30–79%) | 1 sairaudessa |
| UQCRC1ubiquinol-cytochrome c reductase core protein 1 | Usein (30–79%) | 1 sairaudessa |
| VPS35VPS35 retromer complex component | Usein (30–79%) | 2 sairaudessa |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Joskus (5–29%) | 1 sairaudessa |
| ATP13A2ATPase cation transporting 13A2 | Joskus (5–29%) | 1 sairaudessa |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Joskus (5–29%) | 1 sairaudessa |
Näytä 21 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Joskus (5–29%) | 1 sairaudessa |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Joskus (5–29%) | 1 sairaudessa |
| DNMT1DNA methyltransferase 1 | Joskus (5–29%) | 1 sairaudessa |
| GCH1GTP cyclohydrolase 1 | Joskus (5–29%) | 1 sairaudessa |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Joskus (5–29%) | 1 sairaudessa |
| OPA3outer mitochondrial membrane lipid metabolism regulator OPA3 | Joskus (5–29%) | 1 sairaudessa |
| PARK7Parkinsonism associated deglycase | Joskus (5–29%) | 1 sairaudessa |
| TTC19tetratricopeptide repeat domain 19 | Joskus (5–29%) | 1 sairaudessa |
| VPS13Avacuolar protein sorting 13 homolog A | Joskus (5–29%) | 1 sairaudessa |
| FTLferritin light chain | Harvinainen (1–4 %) | 1 sairaudessa |
| MAN1B1mannosidase alpha class 1B member 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| ADH1Calcohol dehydrogenase 1C (class I), gamma polypeptide | Ei kirjattu | 1 sairaudessa |
| ATXN2ataxin 2 | Ei kirjattu | 1 sairaudessa |
| ATXN3ataxin 3 | Ei kirjattu | 1 sairaudessa |
| ATXN8OSATXN8 opposite strand lncRNA | Ei kirjattu | 1 sairaudessa |
| FMR1fragile X messenger ribonucleoprotein 1 | Ei kirjattu | 1 sairaudessa |
| MAPTmicrotubule associated protein tau | Ei kirjattu | 1 sairaudessa |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | Ei kirjattu | 1 sairaudessa |
| PINK1PTEN induced kinase 1 | Ei kirjattu | 1 sairaudessa |
| SNCAIPsynuclein alpha interacting protein | Ei kirjattu | 1 sairaudessa |
| TBPTATA-box binding protein | Ei kirjattu | 1 sairaudessa |
Kuinka usein ilmiö esiintyy ihmisillä, joilla on jokin geenin sairauksista, niin kuin Human Phenotype Ontology sen kirjaa. Nämä sivut kuvaavat piirteitä ja niiden taustalla olevaa tutkimusta, eivätkä ne ole diagnoosi. Oireista kannattaa kysyä lääkäriltä tai geneettiseltä neuvojalta.
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Mistä tämä tieto tulee
- Human Phenotype Ontology, julkaisu 2026-09-01: piirre, sen nimet, määritelmä ja siihen liitetyt geenit. Lue lisää osoitteesta hpo.jax.org.
- Tietojulkaisu 2026.10.19-9814e911.
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Kirjaudu sisäänKysySekvensoi genomisi↗
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