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Træk
Wry neck
Klinisk navn: Torticollis
Involuntary contractions of the neck musculature resulting in an abnormal posture of or abnormal movements of the head.
Resumé
- Også kaldet
- Cervical dystonia, Loxia, Spasmodic torticollis
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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/torticollis.json"
page <- fromJSON(url)
page$trait$nameWry neckHP:0000473
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Læs de gener, der er knyttet til Wry neck, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test50 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.
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 19 of these genesANO3COL6A3TSPOAP1SGCEATP1A3GCH1About this report →
- Congenital Cranial Dysinnervation DisordersReads 5 of these genesCOL25A1KIF21APHOX2ATUBA1ATUBB3About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 6 of these genesCACNA1AAFG3L2ATP1A3TBPTGM6KCNC3About this report →
- TubulinopathiesReads 2 of these genesTUBA1ATUBB3About this report →
Show 46 more reports
- FOXP2-Related Speech and Language DisorderReads 1 of these genesFOXP2About this report →
- GTP Cyclohydrolase 1 DeficiencyReads 1 of these genesGCH1About this report →
- Horizontal Gaze Palsy with Progressive ScoliosisReads 1 of these genesROBO3About this report →
- HPCA-Related DystoniaReads 1 of these genesHPCAAbout this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- Turnpenny-Fry SyndromeReads 1 of these genesPCGF2About this report →
- VPS11-Related LeukodystrophyReads 1 of these genesVPS11About this report →
- Inherited Neurodegenerative DisordersReads 18 of these genesSCP2VPS11CACNA1AAFG3L2ATP1A3GDAP2About this report →
- Congenital Muscular DystrophiesReads 5 of these genesCOL6A3COL12A1COL6A1COL6A2ITGA7About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 3 of these genesTUBA1ATUBB2BTUBB3About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 2 of these genesCACNA1AKMT2BAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesCPATP13A2About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 2 of these genesDDCGCH1About this report →
- Familial Hemiplegic MigraineReads 1 of these genesCACNA1AAbout this report →
- Hereditary Optic NeuropathyReads 2 of these genesAFG3L2ATP1A3About this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesCOL6A3COL6A1COL6A2About this report →
- Hereditary Episodic AtaxiasReads 1 of these genesCACNA1AAbout this report →
- Inherited Iron Metabolism DisordersReads 1 of these genesCPAbout this report →
- Other Inherited LeukodystrophiesReads 4 of these genesSCP2VPS11NKX6-2TUBB4AAbout this report →
- Ehlers-Danlos SyndromeReads 2 of these genesCOL12A1B3GALT6About this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesCEP85LTUBA1AAbout this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesKCNK3About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFB2About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 2 of these genesVPS11TUBB4AAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 3 of these genesGDAP2PRDX3VPS13DAbout this report →
- Waardenburg SyndromeReads 1 of these genesSOX10About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesKIF1CRNF170ATP13A2About this report →
- Epilepsy (Full Panel)Reads 5 of these genesRNU2-2CACNA1AATP1A3SYNGAP1PRRT2About this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 1 of these genesHK1About this report →
- Intellectual DisabilityReads 5 of these genesKDM6BGRIK2NAA10SYNGAP1CDK10About this report →
- Marfan Like SyndromesReads 1 of these genesTGFB2About this report →
- HyperinsulinismReads 1 of these genesHK1About this report →
- Polycystic Kidney DiseaseReads 1 of these genesALG9About this report →
- Aortic AneurysmReads 1 of these genesTGFB2About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Parkinson DiseaseReads 1 of these genesATP13A2About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesPRDX3About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesHK1TRPV4About this report →
- Congenital MyopathiesReads 1 of these genesACTA1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesTRPM3About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesALG9B3GALT6About this report →
- Inherited ThrombocytopeniasReads 1 of these genesFLI1About this report →
- Primary Mitochondrial DiseaseReads 2 of these genesAFG3L2COX20About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesHK1TRPV4About this report →
- Retinitis PigmentosaReads 1 of these genesHK1About this report →
Læs de gener, der er knyttet til Wry neck, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test82 gener knyttet til Wry neck
Ændringer i disse gener forårsager sjældne tilstande, hvor Wry neck 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 |
|---|---|---|
| ANO3anoctamin 3 | Altid | I 2 tilstande |
| COL6A3collagen type VI alpha 3 chain | Altid | I 3 tilstande |
| COX18cytochrome c oxidase assembly factor COX18 | Altid | I 1 tilstand |
| KCNK3potassium two pore domain channel subfamily K member 3 | Altid | I 1 tilstand |
| KDM6Blysine demethylase 6B | Altid | I 1 tilstand |
| MYF5myogenic factor 5 | Altid | I 1 tilstand |
| PGBD5piggyBac transposable element derived 5 | Altid | I 1 tilstand |
| RNU2-2RNA, U2 small nuclear 2 | Altid | I 1 tilstand |
| ROBO3roundabout guidance receptor 3 | Altid | I 1 tilstand |
| SCP2sterol carrier protein 2 | Altid | I 1 tilstand |
| TSPOAP1TSPO associated protein 1 | Altid | I 2 tilstande |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Altid | I 1 tilstand |
| VPS11VPS11 core subunit of CORVET and HOPS complexes | Altid | I 1 tilstand |
| ACTA1actin alpha 1, skeletal muscle | Meget ofte (80–99 %) | I 1 tilstand |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Meget ofte (80–99 %) | I 2 tilstande |
| SGCEsarcoglycan epsilon | Meget ofte (80–99 %) | I 2 tilstande |
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Ofte (30–79 %) | I 2 tilstande |
| CIZ1CDKN1A interacting zinc finger protein 1 | Ofte (30–79 %) | I 1 tilstand |
| COL12A1collagen type XII alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COL6A1collagen type VI alpha 1 chain | Ofte (30–79 %) | I 3 tilstande |
| COL6A2collagen type VI alpha 2 chain | Ofte (30–79 %) | I 2 tilstande |
| COX20cytochrome c oxidase assembly factor COX20 | Ofte (30–79 %) | I 1 tilstand |
| DDCdopa decarboxylase | Ofte (30–79 %) | I 1 tilstand |
| DRD2dopamine receptor D2 | Ofte (30–79 %) | I 1 tilstand |
| GCH1GTP cyclohydrolase 1 | Ofte (30–79 %) | I 2 tilstande |
| GDAP2ganglioside induced differentiation associated protein 2 | Ofte (30–79 %) | I 1 tilstand |
| GNALG protein subunit alpha L | Ofte (30–79 %) | I 2 tilstande |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| HPCAhippocalcin | Ofte (30–79 %) | I 2 tilstande |
| IMPDH2inosine monophosphate dehydrogenase 2 | Ofte (30–79 %) | I 1 tilstand |
| ITGA7integrin subunit alpha 7 | Ofte (30–79 %) | I 1 tilstand |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Ofte (30–79 %) | I 1 tilstand |
| KCTD17potassium channel tetramerization domain containing 17 | Ofte (30–79 %) | I 2 tilstande |
| KMT2Blysine methyltransferase 2B | Ofte (30–79 %) | I 2 tilstande |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Ofte (30–79 %) | I 2 tilstande |
| NEK9NIMA related kinase 9 | Ofte (30–79 %) | I 1 tilstand |
| NKX6-2NK6 homeobox 2 | Ofte (30–79 %) | I 1 tilstand |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Ofte (30–79 %) | I 1 tilstand |
| PRDX3peroxiredoxin 3 | Ofte (30–79 %) | I 1 tilstand |
Vis 42 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | Ofte (30–79 %) | I 1 tilstand |
| SOX10SRY-box transcription factor 10 | Ofte (30–79 %) | I 1 tilstand |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Ofte (30–79 %) | I 1 tilstand |
| TBPTATA-box binding protein | Ofte (30–79 %) | I 1 tilstand |
| TGM6transglutaminase 6 | Ofte (30–79 %) | I 2 tilstande |
| THAP1THAP domain containing 1 | Ofte (30–79 %) | I 2 tilstande |
| TOR1Atorsin family 1 member A | Ofte (30–79 %) | I 2 tilstande |
| TUBB4Atubulin beta 4A class IVa | Ofte (30–79 %) | I 2 tilstande |
| ZNF142zinc finger protein 142 | Ofte (30–79 %) | I 1 tilstand |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| B3GALT6beta-1,3-galactosyltransferase 6 | Nogle gange (5–29 %) | I 1 tilstand |
| CDK10cyclin dependent kinase 10 | Nogle gange (5–29 %) | I 1 tilstand |
| CEP85Lcentrosomal protein 85L | Nogle gange (5–29 %) | I 1 tilstand |
| COL25A1collagen type XXV alpha 1 chain | Nogle gange (5–29 %) | I 1 tilstand |
| CPceruloplasmin | Nogle gange (5–29 %) | I 2 tilstande |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| FOXP2forkhead box P2 | Nogle gange (5–29 %) | I 1 tilstand |
| HK1hexokinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNC3potassium voltage-gated channel subfamily C member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| KIF1Ckinesin family member 1C | Nogle gange (5–29 %) | I 2 tilstande |
| KIF21Akinesin family member 21A | Nogle gange (5–29 %) | I 1 tilstand |
| NAXENAD(P)HX epimerase | Nogle gange (5–29 %) | I 1 tilstand |
| PHLDB1pleckstrin homology like domain family B member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PHOX2Apaired like homeobox 2A | Nogle gange (5–29 %) | I 1 tilstand |
| PNKDPNKD metallo-beta-lactamase domain containing | Nogle gange (5–29 %) | I 2 tilstande |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Nogle gange (5–29 %) | I 1 tilstand |
| PRRT2proline rich transmembrane protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| RNF170ring finger protein 170 | Nogle gange (5–29 %) | I 1 tilstand |
| SUPT16HSPT16 homolog, facilitates chromatin remodeling subunit | Nogle gange (5–29 %) | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM151Atransmembrane protein 151A | Nogle gange (5–29 %) | I 1 tilstand |
| TRPM3transient receptor potential cation channel subfamily M member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TUBA1Atubulin alpha 1a | Nogle gange (5–29 %) | I 1 tilstand |
| TUBB2Btubulin beta 2B class IIb | Nogle gange (5–29 %) | I 1 tilstand |
| TUBB3tubulin beta 3 class III | Nogle gange (5–29 %) | I 2 tilstande |
| VPS13Dvacuolar protein sorting 13 homolog D | Nogle gange (5–29 %) | I 1 tilstand |
| VPS16VPS16 core subunit of CORVET and HOPS complexes | Nogle gange (5–29 %) | I 1 tilstand |
| SPTBN1spectrin beta, non-erythrocytic 1 | Sjældent (1–4%) | I 1 tilstand |
| ATP13A2ATPase cation transporting 13A2 | Ikke registreret | I 1 tilstand |
| COLEC11collectin subfamily member 11 | Ikke registreret | I 1 tilstand |
| PCGF2polycomb group ring finger 2 | Ikke registreret | I 1 tilstand |
| TRPV4transient receptor potential cation channel subfamily V member 4 | 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.
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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.
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Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
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