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Træk
Involuntary movements
Involuntary contractions of muscle leading to involuntary movements of extremities, neck, trunk, or face.
Resumé
- Også kaldet
- Involuntary muscle contractions
- Kropssystem
- Abnormality of the nervous system
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/involuntary-movements.json"
page <- fromJSON(url)
page$trait$nameInvoluntary movementsHP:0004305
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Læs de gener, der er knyttet til Involuntary movements, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test56 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.
- Epilepsy (Full Panel)Reads 63 of these genesSYNJ1CDKL5GABBR2KCNA1MECP2PRRT2About this report →
- Basal Ganglia CalcificationReads 7 of these genesJAM2MYORGNAA60PDGFBPDGFRBSLC20A2About this report →
- Familial Hemiplegic MigraineReads 3 of these genesATP1A2CACNA1ASCN1AAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 10 of these genesKCNJ10PRRT2HPCAPNKDSLC2A1TMEM151AAbout this report →
Show 52 more reports
- Hereditary Episodic AtaxiasReads 3 of these genesKCNA1CACNA1ASCN2AAbout this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 2 of these genesVPS13AJPH3About this report →
- ADCY5-Related DyskinesiaReads 1 of these genesADCY5About this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- DHX30-Related Neurodevelopmental DisorderReads 1 of these genesDHX30About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- HPCA-Related DystoniaReads 1 of these genesHPCAAbout this report →
- Huntington DiseaseReads 1 of these genesHTTAbout this report →
- KCNQ2-Related Neonatal Encephalopathy with Non-Epileptic MyoclonusReads 1 of these genesKCNQ2About this report →
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Inherited Neurodegenerative DisordersReads 16 of these genesTWNKVPS13AATN1CACNA1ACPFTLAbout this report →
- Intellectual DisabilityReads 12 of these genesDEAF1MECP2GRIK2GRIN1SCN2ACAMK2AAbout this report →
- Parkinson DiseaseReads 3 of these genesSYNJ1DNAJC6MAPTAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 4 of these genesATN1CACNA1ATBPATP1A3About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 2 of these genesCACNA1ACACNA1BAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesCPFTLAbout this report →
- Primary Mitochondrial DiseaseReads 6 of these genesTWNKDNAJC30AIFM1CARS2GFM2LIG3About this report →
- Cutis LaxaReads 2 of these genesELNATP6V1AAbout this report →
- Inherited Iron Metabolism DisordersReads 1 of these genesCPAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesVPS13AAIFM1IARS2AARS1GFM2LIG3About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 2 of these genesCHMP1ATOE1About this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesCEP85LMACF1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Cornelia de Lange SyndromeReads 1 of these genesSMC1AAbout this report →
- Leigh SyndromeReads 3 of these genesAIFM1GFM2MECRAbout this report →
- Congenital Disorders of GlycosylationReads 3 of these genesPGAP3DHDDSNUS1About this report →
- Familial HypomagnesemiaReads 1 of these genesKCNJ10About this report →
- Frontotemporal DementiaReads 1 of these genesMAPTAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesATP1A3About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Congenital Stationary Night BlindnessReads 1 of these genesCABP4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesAIFM1AARS1About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesAARS1TUBB4AAbout this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPGAP3About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesAIFM1About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesFTLAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesZFXAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesTUBB4AAbout this report →
- Nephrotic SyndromeReads 1 of these genesPODXLAbout this report →
- Thyroid CancerReads 1 of these genesGNASAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTWNKAbout this report →
- Retinitis PigmentosaReads 1 of these genesDHDDSAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesAIFM1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNCF1About this report →
Læs de gener, der er knyttet til Involuntary movements, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test143 gener knyttet til Involuntary movements
Ændringer i disse gener forårsager sjældne tilstande, hvor Involuntary movements ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| DEAF1DEAF1 transcription factor | Altid | I 2 tilstande |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Altid | I 2 tilstande |
| SYNJ1synaptojanin 1 | Altid | I 3 tilstande |
| TWNKtwinkle mtDNA helicase | Altid | I 1 tilstand |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Meget ofte (80–99 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Meget ofte (80–99 %) | I 1 tilstand |
| CDKL5cyclin dependent kinase like 5 | Meget ofte (80–99 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Meget ofte (80–99 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Meget ofte (80–99 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Meget ofte (80–99 %) | I 1 tilstand |
| ELNelastin | Meget ofte (80–99 %) | I 1 tilstand |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Meget ofte (80–99 %) | I 1 tilstand |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Meget ofte (80–99 %) | I 2 tilstande |
| GTF2Igeneral transcription factor IIi | Meget ofte (80–99 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Meget ofte (80–99 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Meget ofte (80–99 %) | I 1 tilstand |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Meget ofte (80–99 %) | I 1 tilstand |
| LIMK1LIM domain kinase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Meget ofte (80–99 %) | I 2 tilstande |
| METTL27methyltransferase like 27 | Meget ofte (80–99 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Meget ofte (80–99 %) | I 1 tilstand |
| NGLY1N-glycanase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| NTNG1netrin G1 | Meget ofte (80–99 %) | I 1 tilstand |
| PRRT2proline rich transmembrane protein 2 | Meget ofte (80–99 %) | I 5 tilstande |
| RFC2replication factor C subunit 2 | Meget ofte (80–99 %) | I 1 tilstand |
| SMC1Astructural maintenance of chromosomes 1A | Meget ofte (80–99 %) | I 1 tilstand |
| STX1Asyntaxin 1A | Meget ofte (80–99 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Meget ofte (80–99 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Meget ofte (80–99 %) | I 1 tilstand |
| VPS13Avacuolar protein sorting 13 homolog A | Meget ofte (80–99 %) | I 1 tilstand |
| VPS37DVPS37D subunit of ESCRT-I | Meget ofte (80–99 %) | I 1 tilstand |
| ADCY5adenylate cyclase 5 | Ofte (30–79 %) | I 1 tilstand |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Ofte (30–79 %) | I 2 tilstande |
| ATN1atrophin 1 | Ofte (30–79 %) | I 1 tilstand |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Ofte (30–79 %) | I 2 tilstande |
| CABP4calcium binding protein 4 | Ofte (30–79 %) | I 1 tilstand |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Ofte (30–79 %) | I 2 tilstande |
| CEP85Lcentrosomal protein 85L | Ofte (30–79 %) | I 1 tilstand |
| CHRNA2cholinergic receptor nicotinic alpha 2 subunit | Ofte (30–79 %) | I 1 tilstand |
Vis 103 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| CHRNA4cholinergic receptor nicotinic alpha 4 subunit | Ofte (30–79 %) | I 1 tilstand |
| CHRNB2cholinergic receptor nicotinic beta 2 subunit | Ofte (30–79 %) | I 1 tilstand |
| CPceruloplasmin | Ofte (30–79 %) | I 1 tilstand |
| CRHcorticotropin releasing hormone | Ofte (30–79 %) | I 1 tilstand |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Ofte (30–79 %) | I 2 tilstande |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Ofte (30–79 %) | I 1 tilstand |
| DNM1dynamin 1 | Ofte (30–79 %) | I 2 tilstande |
| FTLferritin light chain | Ofte (30–79 %) | I 1 tilstand |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| HPCAhippocalcin | Ofte (30–79 %) | I 1 tilstand |
| HTThuntingtin | Ofte (30–79 %) | I 1 tilstand |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Ofte (30–79 %) | I 1 tilstand |
| KCNQ3potassium voltage-gated channel subfamily Q member 3 | Ofte (30–79 %) | I 1 tilstand |
| KCNT1potassium sodium-activated channel subfamily T member 1 | Ofte (30–79 %) | I 1 tilstand |
| MACF1microtubule actin crosslinking factor 1 | Ofte (30–79 %) | I 2 tilstande |
| MAPTmicrotubule associated protein tau | Ofte (30–79 %) | I 1 tilstand |
| MICU1mitochondrial calcium uptake 1 | Ofte (30–79 %) | I 1 tilstand |
| PGAP3post-GPI attachment to proteins phospholipase 3 | Ofte (30–79 %) | I 1 tilstand |
| PNKDPNKD metallo-beta-lactamase domain containing | Ofte (30–79 %) | I 1 tilstand |
| PODXLpodocalyxin like | Ofte (30–79 %) | I 1 tilstand |
| PRNPprion protein (Kanno blood group) | Ofte (30–79 %) | I 1 tilstand |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Ofte (30–79 %) | I 2 tilstande |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Ofte (30–79 %) | I 2 tilstande |
| SLC2A1solute carrier family 2 member 1 | Ofte (30–79 %) | I 1 tilstand |
| SLC2A3solute carrier family 2 member 3 | Ofte (30–79 %) | I 1 tilstand |
| TANGO2transport and golgi organization 2 homolog | Ofte (30–79 %) | I 1 tilstand |
| TBPTATA-box binding protein | Ofte (30–79 %) | I 1 tilstand |
| TMEM151Atransmembrane protein 151A | Ofte (30–79 %) | I 1 tilstand |
| AARS1alanyl-tRNA synthetase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ACTL6Bactin like 6B | Nogle gange (5–29 %) | I 1 tilstand |
| AP3B2adaptor related protein complex 3 subunit beta 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Nogle gange (5–29 %) | I 1 tilstand |
| ATP6V1AATPase H+ transporting V1 subunit A | Nogle gange (5–29 %) | I 1 tilstand |
| CACNA1Bcalcium voltage-gated channel subunit alpha1 B | Nogle gange (5–29 %) | I 1 tilstand |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CAMK2Acalcium/calmodulin dependent protein kinase II alpha | Nogle gange (5–29 %) | I 1 tilstand |
| CARS2cysteinyl-tRNA synthetase 2, mitochondrial | Nogle gange (5–29 %) | I 1 tilstand |
| CDK19cyclin dependent kinase 19 | Nogle gange (5–29 %) | I 1 tilstand |
| CELF2CUGBP Elav-like family member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| CHMP1Acharged multivesicular body protein 1A | Nogle gange (5–29 %) | I 1 tilstand |
| CLTCclathrin heavy chain | Nogle gange (5–29 %) | I 1 tilstand |
| CMPK2cytidine/uridine monophosphate kinase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| CNKSR2connector enhancer of kinase suppressor of Ras 2 | Nogle gange (5–29 %) | I 1 tilstand |
| CYFIP2cytoplasmic FMR1 interacting protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| DALRD3DALR anticodon binding domain containing 3 | Nogle gange (5–29 %) | I 1 tilstand |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Nogle gange (5–29 %) | I 1 tilstand |
| EEF1A2eukaryotic translation elongation factor 1 alpha 2 | Nogle gange (5–29 %) | I 1 tilstand |
| FBXO28F-box protein 28 | Nogle gange (5–29 %) | I 1 tilstand |
| FGF12fibroblast growth factor 12 | Nogle gange (5–29 %) | I 1 tilstand |
| FOXG1forkhead box G1 | Nogle gange (5–29 %) | I 1 tilstand |
| FZR1fizzy and cell division cycle 20 related 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRA2gamma-aminobutyric acid type A receptor subunit alpha2 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRA5gamma-aminobutyric acid type A receptor subunit alpha5 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRB2gamma-aminobutyric acid type A receptor subunit beta2 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Nogle gange (5–29 %) | I 1 tilstand |
| GFM2GTP dependent ribosome recycling factor mitochondrial 2 | Nogle gange (5–29 %) | I 2 tilstande |
| GNASGNAS complex locus | Nogle gange (5–29 %) | I 1 tilstand |
| GRIN2Dglutamate ionotropic receptor NMDA type subunit 2D | Nogle gange (5–29 %) | I 1 tilstand |
| HCN1hyperpolarization activated cyclic nucleotide gated potassium channel 1 | Nogle gange (5–29 %) | I 1 tilstand |
| JAM2junctional adhesion molecule 2 | Nogle gange (5–29 %) | I 1 tilstand |
| JPH3junctophilin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNA2potassium voltage-gated channel subfamily A member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNB1potassium voltage-gated channel subfamily B member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNC2potassium voltage-gated channel subfamily C member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNH5potassium voltage-gated channel subfamily H member 5 | Nogle gange (5–29 %) | I 1 tilstand |
| LIG3DNA ligase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| MYORGmyogenesis regulating glycosidase | Nogle gange (5–29 %) | I 1 tilstand |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Nogle gange (5–29 %) | I 1 tilstand |
| NECAP1NECAP endocytosis associated 1 | Nogle gange (5–29 %) | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| NTRK2neurotrophic receptor tyrosine kinase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| NUS1NUS1 dehydrodolichyl diphosphate synthase subunit | Nogle gange (5–29 %) | I 1 tilstand |
| PACS2phosphofurin acidic cluster sorting protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| PARS2prolyl-tRNA synthetase 2, mitochondrial | Nogle gange (5–29 %) | I 1 tilstand |
| PDGFBplatelet derived growth factor subunit B | Nogle gange (5–29 %) | I 1 tilstand |
| PDGFRBplatelet derived growth factor receptor beta | Nogle gange (5–29 %) | I 1 tilstand |
| PPP3CAprotein phosphatase 3 catalytic subunit alpha | Nogle gange (5–29 %) | I 1 tilstand |
| RRP12ribosomal RNA processing 12 homolog | Nogle gange (5–29 %) | I 1 tilstand |
| SCN3Asodium voltage-gated channel alpha subunit 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC13A5solute carrier family 13 member 5 | Nogle gange (5–29 %) | I 2 tilstande |
| SLC1A2solute carrier family 1 member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC20A2solute carrier family 20 member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC38A3solute carrier family 38 member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SMSspermine synthase | Nogle gange (5–29 %) | I 1 tilstand |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SZT2SZT2 subunit of KICSTOR complex | Nogle gange (5–29 %) | I 1 tilstand |
| TOE1target of EGR1, exonuclease | Nogle gange (5–29 %) | I 1 tilstand |
| TRAK1trafficking kinesin protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TUBB4Atubulin beta 4A class IVa | Nogle gange (5–29 %) | I 1 tilstand |
| UBA5ubiquitin like modifier activating enzyme 5 | Nogle gange (5–29 %) | I 1 tilstand |
| UFSP2UFM1 specific peptidase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Nogle gange (5–29 %) | I 2 tilstande |
| YWHAGtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma | Nogle gange (5–29 %) | I 1 tilstand |
| ZFXzinc finger protein X-linked | Nogle gange (5–29 %) | I 1 tilstand |
| DHX30DExH-box helicase 30 | Ikke registreret | I 1 tilstand |
| GNAO1G protein subunit alpha o1 | Ikke registreret | I 1 tilstand |
| GPR88G protein-coupled receptor 88 | Ikke registreret | I 1 tilstand |
| MECRmitochondrial trans-2-enoyl-CoA reductase | Ikke registreret | I 1 tilstand |
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | Ikke registreret | I 1 tilstand |
| SYT1synaptotagmin 1 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Snævrere træk
- Tremor495 gener
- Jerking352 gener
- Chorea189 gener
- Clonus98 gener
- Muscle twitch91 gener
- Involuntary writhing movements in fingers, hands, toes, and feet69 gener
- Paroxysmal dyskinesia22 gener
- Alien limb phenomenon4 gener
- Hemiballismus4 gener
- Akathisia1 gen
- Chvostek sign1 gen
- Self-mutilation of tongue and lips due to involuntary movements1 gen
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
AtlasHvem vi hjælperVores videnskabProdukterResultater
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Read the genes behind these traits in your own DNA.
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