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PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Clumsiness
Lack of physical coordination resulting in an abnormal tendency to drop items or bump into objects.
Santrauka
- Kūno sistema
- Abnormality of the nervous system
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/clumsiness.json"
page <- fromJSON(url)
page$trait$nameClumsinessHP:0002312
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Clumsiness, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test59 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.
- Basal Ganglia CalcificationReads 7 of these genesJAM2MYORGNAA60PDGFBPDGFRBSLC20A2About this report →
- Congenital MyopathiesReads 8 of these genesACTA1KBTBD13KLHL41MYPNNEBTPM2About this report →
- Megalencephalic Leukoencephalopathy with Subcortical CystsReads 3 of these genesGPRC5BHEPACAMMLC1About this report →
- Metachromatic LeukodystrophyReads 2 of these genesARSAPSAPAbout this report →
Show 55 more reports
- Riboflavin Transporter DeficiencyReads 2 of these genesSLC52A2SLC52A3About this report →
- Lysosomal Storage DiseaseReads 8 of these genesARSAASAH1CLN8GALCPSAPTPP1About this report →
- Other Inherited LeukodystrophiesReads 9 of these genesGPRC5BARSADARS2GALCHEPACAMPOLR3AAbout this report →
- Angelman SyndromeReads 1 of these genesUBE3AAbout this report →
- Friedreich AtaxiaReads 1 of these genesFXNAbout this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)Reads 1 of these genesPMP22About this report →
- Huntington DiseaseReads 1 of these genesHTTAbout this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 7 of these genesCWF19L1TTPAFXNTPP1RNF168SYNE1About this report →
- Bartter DiseaseReads 2 of these genesBSNDCLCNKBAbout this report →
- Frontotemporal DementiaReads 3 of these genesHNRNPA1SQSTM1MAPTAbout this report →
- Neuronal Ceroid LipofuscinosisReads 3 of these genesCLN8TPP1CLN5About this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Hereditary Manganese Transporter DisordersReads 1 of these genesSLC39A14About this report →
- Distal MyopathiesReads 3 of these genesHNRNPA1TIA1TTNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 6 of these genesSPTAN1GJB1MPZPMP22SCO2MORC2About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesPLA2G6PANK2About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- Parkinson DiseaseReads 2 of these genesPLA2G6MAPTAbout this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesCAPN3CAV3TTNAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 3 of these genesNR4A2CLCN1MECRAbout this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- GalactosemiaReads 1 of these genesGALTAbout this report →
- Hereditary Episodic AtaxiasReads 1 of these genesKCNA1About this report →
- Leigh SyndromeReads 4 of these genesPDHA1SCO2SDHAMECRAbout this report →
- Congenital HypothyroidismReads 2 of these genesNKX2-1TSHBAbout this report →
- Epilepsy (Full Panel)Reads 6 of these genesPAK3SPTAN1CLN8KCNA1ALG13GRIN2AAbout this report →
- Dilated CardiomyopathyReads 3 of these genesMYPNSYNE1TTNAbout this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesACOX1About this report →
- Intellectual DisabilityReads 6 of these genesCHD8PAK3AFF2CLTCDEAF1KDM4BAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesSPTAN1ASAH1About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesMAN2B1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesHNRNPA1SQSTM1About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesSDHAAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesATXN3KCNC3About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesPDHA1About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesSDHAAbout this report →
- Severe Congenital NeutropeniaReads 1 of these genesHAX1About this report →
- Urinary and Renal System TumourReads 1 of these genesSDHAAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesDNM1LAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesTTNAbout this report →
- Female InfertilityReads 2 of these genesGALTTWNKAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesSLC22A5About this report →
- Fanconi AnemiaReads 1 of these genesRAD51About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Thyroid CancerReads 1 of these genesTSHBAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesPOLR3AAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesSCO2TWNKAbout this report →
- DNA Repair DiseaseReads 1 of these genesRAD51About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMYPNAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesSPTAN1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesALG13About this report →
Vienu tyrimu sužinokite genus, susijusius su Clumsiness, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test102 genų susiję su Clumsiness
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Clumsiness. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| AQP4aquaporin 4 | Visada | 2 ligose |
| CHD8chromodomain helicase DNA binding protein 8 | Visada | 1 ligoje |
| CWF19L1CWF19 like cell cycle control factor 1 | Visada | 2 ligose |
| DNM1Ldynamin 1L | Visada | 1 ligoje |
| FDXRferredoxin reductase | Visada | 1 ligoje |
| GPRC5BG protein-coupled receptor class C group 5 member B | Visada | 2 ligose |
| HAX1HCLS1 associated protein X-1 | Visada | 1 ligoje |
| LRRC7leucine rich repeat containing 7 | Visada | 1 ligoje |
| MICU1mitochondrial calcium uptake 1 | Visada | 1 ligoje |
| MSL2MSL complex subunit 2 | Visada | 1 ligoje |
| PAK3p21 (RAC1) activated kinase 3 | Visada | 1 ligoje |
| PDHA1pyruvate dehydrogenase E1 subunit alpha 1 | Visada | 1 ligoje |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Visada | 1 ligoje |
| RAB32RAB32, member RAS oncogene family | Visada | 1 ligoje |
| SPTAN1spectrin alpha, non-erythrocytic 1 | Visada | 1 ligoje |
| TTPAalpha tocopherol transfer protein | Visada | 2 ligose |
| ATP7BATPase copper transporting beta | Labai dažnai (80–99%) | 1 ligoje |
| BCKDKbranched chain keto acid dehydrogenase kinase | Labai dažnai (80–99%) | 1 ligoje |
| SLC22A5solute carrier family 22 member 5 | Labai dažnai (80–99%) | 1 ligoje |
| UBE3Aubiquitin protein ligase E3A | Labai dažnai (80–99%) | 1 ligoje |
| AASSaminoadipate-semialdehyde synthase | Dažnai (30–79%) | 2 ligose |
| ACTA1actin alpha 1, skeletal muscle | Dažnai (30–79%) | 1 ligoje |
| AFF2ALF transcription elongation factor 2 | Dažnai (30–79%) | 1 ligoje |
| ARSAarylsulfatase A | Dažnai (30–79%) | 3 ligose |
| ASAH1N-acylsphingosine amidohydrolase 1 | Dažnai (30–79%) | 1 ligoje |
| ATP2B3ATPase plasma membrane Ca2+ transporting 3 | Dažnai (30–79%) | 1 ligoje |
| ATXN3ataxin 3 | Dažnai (30–79%) | 3 ligose |
| CAPN3calpain 3 | Dažnai (30–79%) | 1 ligoje |
| CLN8CLN8 transmembrane ER and ERGIC protein | Dažnai (30–79%) | 2 ligose |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Dažnai (30–79%) | 1 ligoje |
| DCCDCC netrin 1 receptor | Dažnai (30–79%) | 1 ligoje |
| DNAL4dynein axonemal light chain 4 | Dažnai (30–79%) | 1 ligoje |
| FXNfrataxin | Dažnai (30–79%) | 1 ligoje |
| GALCgalactosylceramidase | Dažnai (30–79%) | 2 ligose |
| GJB1gap junction protein beta 1 | Dažnai (30–79%) | 1 ligoje |
| HEPACAMhepatic and glial cell adhesion molecule | Dažnai (30–79%) | 2 ligose |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Dažnai (30–79%) | 2 ligose |
| HTThuntingtin | Dažnai (30–79%) | 1 ligoje |
| KBTBD13kelch repeat and BTB domain containing 13 | Dažnai (30–79%) | 1 ligoje |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Dažnai (30–79%) | 1 ligoje |
Rodyti dar 62 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| KLHL41kelch like family member 41 | Dažnai (30–79%) | 1 ligoje |
| MPZmyelin protein zero | Dažnai (30–79%) | 1 ligoje |
| MYPNmyopalladin | Dažnai (30–79%) | 1 ligoje |
| NEBnebulin | Dažnai (30–79%) | 1 ligoje |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Dažnai (30–79%) | 1 ligoje |
| NTN1netrin 1 | Dažnai (30–79%) | 1 ligoje |
| PLA2G6phospholipase A2 group VI | Dažnai (30–79%) | 2 ligose |
| PMP22peripheral myelin protein 22 | Dažnai (30–79%) | 1 ligoje |
| POLR3ARNA polymerase III subunit A | Dažnai (30–79%) | 1 ligoje |
| PRNPprion protein (Kanno blood group) | Dažnai (30–79%) | 2 ligose |
| PSAPprosaposin | Dažnai (30–79%) | 3 ligose |
| RAD51RAD51 recombinase | Dažnai (30–79%) | 1 ligoje |
| SCO2synthesis of cytochrome C oxidase 2 | Dažnai (30–79%) | 1 ligoje |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Dažnai (30–79%) | 1 ligoje |
| SKOR2SKI family transcriptional corepressor 2 | Dažnai (30–79%) | 1 ligoje |
| SLC2A3solute carrier family 2 member 3 | Dažnai (30–79%) | 1 ligoje |
| SQSTM1sequestosome 1 | Dažnai (30–79%) | 1 ligoje |
| TIA1TIA1 cytotoxic granule associated RNA binding protein | Dažnai (30–79%) | 1 ligoje |
| TPM2tropomyosin 2 | Dažnai (30–79%) | 1 ligoje |
| TPM3tropomyosin 3 | Dažnai (30–79%) | 1 ligoje |
| TPP1tripeptidyl peptidase 1 | Dažnai (30–79%) | 2 ligose |
| ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunit | Kartais (5–29%) | 1 ligoje |
| BSNDbarttin CLCNK type accessory subunit beta | Kartais (5–29%) | 1 ligoje |
| CACHD1cache domain containing 1 | Kartais (5–29%) | 1 ligoje |
| CAV3caveolin 3 | Kartais (5–29%) | 1 ligoje |
| CLCN1chloride voltage-gated channel 1 | Kartais (5–29%) | 1 ligoje |
| CLCNKAchloride voltage-gated channel Ka | Kartais (5–29%) | 1 ligoje |
| CLCNKBchloride voltage-gated channel Kb | Kartais (5–29%) | 1 ligoje |
| CLTCclathrin heavy chain | Kartais (5–29%) | 1 ligoje |
| CMPK2cytidine/uridine monophosphate kinase 2 | Kartais (5–29%) | 1 ligoje |
| DEAF1DEAF1 transcription factor | Kartais (5–29%) | 1 ligoje |
| GALTgalactose-1-phosphate uridylyltransferase | Kartais (5–29%) | 1 ligoje |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Kartais (5–29%) | 1 ligoje |
| JAM2junctional adhesion molecule 2 | Kartais (5–29%) | 1 ligoje |
| KCNC3potassium voltage-gated channel subfamily C member 3 | Kartais (5–29%) | 1 ligoje |
| KDM4Blysine demethylase 4B | Kartais (5–29%) | 1 ligoje |
| MAN2B1mannosidase alpha class 2B member 1 | Kartais (5–29%) | 2 ligose |
| MAPTmicrotubule associated protein tau | Kartais (5–29%) | 1 ligoje |
| MECRmitochondrial trans-2-enoyl-CoA reductase | Kartais (5–29%) | 1 ligoje |
| MLC1modulator of VRAC current 1 | Kartais (5–29%) | 1 ligoje |
| MORC2MORC family CW-type zinc finger 2 | Kartais (5–29%) | 1 ligoje |
| MYORGmyogenesis regulating glycosidase | Kartais (5–29%) | 1 ligoje |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Kartais (5–29%) | 1 ligoje |
| NKX2-1NK2 homeobox 1 | Kartais (5–29%) | 1 ligoje |
| PDGFBplatelet derived growth factor subunit B | Kartais (5–29%) | 1 ligoje |
| PDGFRBplatelet derived growth factor receptor beta | Kartais (5–29%) | 1 ligoje |
| RNF125ring finger protein 125 | Kartais (5–29%) | 1 ligoje |
| RNF168ring finger protein 168 | Kartais (5–29%) | 1 ligoje |
| RRP12ribosomal RNA processing 12 homolog | Kartais (5–29%) | 1 ligoje |
| SLC20A2solute carrier family 20 member 2 | Kartais (5–29%) | 1 ligoje |
| SLC39A14solute carrier family 39 member 14 | Kartais (5–29%) | 1 ligoje |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Kartais (5–29%) | 1 ligoje |
| TSHBthyroid stimulating hormone subunit beta | Kartais (5–29%) | 1 ligoje |
| TTNtitin | Kartais (5–29%) | 1 ligoje |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Kartais (5–29%) | 1 ligoje |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Retai (1–4 %) | 1 ligoje |
| PANK2pantothenate kinase 2 | Retai (1–4 %) | 1 ligoje |
| ACOX1acyl-CoA oxidase 1 | Neužfiksuota | 1 ligoje |
| CLN5CLN5 lysosomal BMP synthase | Neužfiksuota | 1 ligoje |
| SLC52A2solute carrier family 52 member 2 | Neužfiksuota | 1 ligoje |
| SLC52A3solute carrier family 52 member 3 | Neužfiksuota | 1 ligoje |
| TWNKtwinkle mtDNA helicase | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Platesni požymiai
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- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.18-e609d43e.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
From traits to your genome
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 470+ physician-ready reports.
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Nemokamas pristatymas · Rezultatai per 6–8 savaites
