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PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Nerve damage causing decreased feeling and movement
Klinikinis pavadinimas: Sensorimotor neuropathy
Santrauka
- Taip pat vadinama
- Mixed polyneuropathy, Sensorimotor peripheral neuropathy
- 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/sensorimotor-neuropathy.json"
page <- fromJSON(url)
page$trait$nameKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Nerve damage causing decreased feeling and movement, ir kitą jūsų genomo dalį.
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Įsigyti savo 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.
- Rare Hereditary Peripheral NeuropathiesReads 50 of these genesCLCF1LITAFPOLGRAB7ASPTLC2TYMPAbout this report →
- Charcot-Marie-Tooth DiseaseReads 21 of these genesLITAFRAB7AAIFM1GDAP1MMENEFLAbout this report →
- Inherited Neurodegenerative DisordersReads 39 of these genesAFG3L2POLGXRCC1GALCPSAPSETXAbout this report →
- Hereditary Optic NeuropathyReads 7 of these genesAFG3L2DNM1LMT-ND1MT-ND4MT-ND5MT-ND6About this report →
Show 52 more reports
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 10 of these genesXRCC1SETXPEX6RFC1SACSTDP1About this report →
- Leigh SyndromeReads 11 of these genesAIFM1MT-ATP6MT-ND1MT-ND3MT-ND4MT-ND5About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 3 of these genesHSD17B4AMACRPHYHAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 5 of these genesCLCF1SPTLC2AIFM1KIF1ARFC1About this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)Reads 1 of these genesPMP22About this report →
- KIF5A-Related Amyotrophic Lateral SclerosisReads 1 of these genesKIF5AAbout this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- MCM3AP-Related Peripheral NeuropathyReads 1 of these genesMCM3APAbout this report →
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- OPA1-Related Optic AtrophyReads 1 of these genesOPA1About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Hereditary Spastic ParaplegiaReads 8 of these genesSPG11TFGABCD1B4GALNT1GBA2KIF1AAbout this report →
- Primary Mitochondrial DiseaseReads 11 of these genesAFG3L2POLGTYMPAIFM1LIG3RRM2BAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 4 of these genesSPTLC2SETXSPG11VCPAbout this report →
- Encephalopathy due to Mitochondrial and Peroxisomal Fission DefectReads 1 of these genesDNM1LAbout this report →
- Hereditary Manganese Transporter DisordersReads 1 of these genesSLC30A10About this report →
- Metachromatic LeukodystrophyReads 1 of these genesPSAPAbout this report →
- Riboflavin Transporter DeficiencyReads 1 of these genesSLC52A2About this report →
- Other Inherited LeukodystrophiesReads 6 of these genesGALCPSAPABCD1PEX6PEX7RPIAAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 3 of these genesCLP1SLC25A46VRK1About this report →
- Spinal Muscular AtrophyReads 3 of these genesEMILIN1VRK1IGHMBP2About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 2 of these genesPEX6PEX7About this report →
- Parkinson DiseaseReads 2 of these genesPLA2G6GBA1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 3 of these genesAFG3L2PPP2R2BPDYNAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 2 of these genesHADHAHADHBAbout this report →
- DNA Repair DiseaseReads 3 of these genesSETXTDP1MRE11About this report →
- Lysosomal Storage DiseaseReads 3 of these genesGALCPSAPGBA1About this report →
- Hepatic Porphyria DisordersReads 1 of these genesHMBSAbout this report →
- PorphyriaReads 1 of these genesHMBSAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesPLA2G6About this report →
- Familial HypomagnesemiaReads 1 of these genesATP1A1About this report →
- Hereditary AmyloidosisReads 1 of these genesB2MAbout this report →
- Frontotemporal DementiaReads 1 of these genesVCPAbout this report →
- Hypertrophic CardiomyopathyReads 2 of these genesDHHHADHAAbout this report →
- Cutis LaxaReads 1 of these genesEMILIN1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesDHHAbout this report →
- Distal MyopathiesReads 1 of these genesVCPAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGBAbout this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesAHCYAbout this report →
- Epilepsy (Full Panel)Reads 3 of these genesPNKPSCARB2PIGBAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesLAMA2About this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLAMA2About this report →
- Osteogenesis ImperfectaReads 1 of these genesPPIBAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesADA2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPNKPAbout this report →
- Female InfertilityReads 1 of these genesHSD17B4About this report →
- Intellectual DisabilityReads 2 of these genesKIF1AVRK1About this report →
- Hearing Loss and DeafnessReads 1 of these genesAIFM1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesB2MAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Nerve damage causing decreased feeling and movement, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test107 genų susiję su Nerve damage causing decreased feeling and movement
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Nerve damage causing decreased feeling and movement. 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 |
|---|---|---|
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Visada | 2 ligose |
| ARHGAP19Rho GTPase activating protein 19 | Visada | 1 ligoje |
| CLCF1cardiotrophin like cytokine factor 1 | Visada | 1 ligoje |
| COA3cytochrome c oxidase assembly factor 3 | Visada | 1 ligoje |
| GET4guided entry of tail-anchored proteins factor 4 | Visada | 1 ligoje |
| HMBShydroxymethylbilane synthase | Visada | 2 ligose |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Visada | 1 ligoje |
| LAMA2laminin subunit alpha 2 | Visada | 2 ligose |
| LITAFlipopolysaccharide induced TNF factor | Visada | 1 ligoje |
| MCM3APminichromosome maintenance complex component 3 associated protein | Visada | 1 ligoje |
| POLGDNA polymerase gamma, catalytic subunit | Visada | 2 ligose |
| RAB7ARAB7A, member RAS oncogene family | Visada | 1 ligoje |
| RCC1regulator of chromosome condensation 1 | Visada | 1 ligoje |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Visada | 1 ligoje |
| TYMPthymidine phosphorylase | Visada | 2 ligose |
| XRCC1X-ray repair cross complementing 1 | Visada | 1 ligoje |
| ADA2adenosine deaminase 2 | Labai dažnai (80–99%) | 1 ligoje |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Labai dažnai (80–99%) | 1 ligoje |
| DHHdesert hedgehog signaling molecule | Labai dažnai (80–99%) | 1 ligoje |
| GALCgalactosylceramidase | Labai dažnai (80–99%) | 4 ligose |
| GDAP1ganglioside induced differentiation associated protein 1 | Labai dažnai (80–99%) | 1 ligoje |
| LIG3DNA ligase 3 | Labai dažnai (80–99%) | 1 ligoje |
| MMEmembrane metalloendopeptidase | Labai dažnai (80–99%) | 3 ligose |
| NEFLneurofilament light chain | Labai dažnai (80–99%) | 3 ligose |
| NGLY1N-glycanase 1 | Labai dažnai (80–99%) | 1 ligoje |
| PDK3pyruvate dehydrogenase kinase 3 | Labai dažnai (80–99%) | 1 ligoje |
| PIK3R5phosphoinositide-3-kinase regulatory subunit 5 | Labai dažnai (80–99%) | 1 ligoje |
| PSAPprosaposin | Labai dažnai (80–99%) | 1 ligoje |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Labai dažnai (80–99%) | 2 ligose |
| SETXsenataxin | Labai dažnai (80–99%) | 1 ligoje |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Labai dažnai (80–99%) | 1 ligoje |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Labai dažnai (80–99%) | 1 ligoje |
| TFGtrafficking from ER to golgi regulator | Labai dažnai (80–99%) | 1 ligoje |
| ABCD1ATP binding cassette subfamily D member 1 | Dažnai (30–79%) | 1 ligoje |
| AMACRalpha-methylacyl-CoA racemase | Dažnai (30–79%) | 2 ligose |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Dažnai (30–79%) | 1 ligoje |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Dažnai (30–79%) | 1 ligoje |
| COA8cytochrome c oxidase assembly factor 8 | Dažnai (30–79%) | 1 ligoje |
| DNAJC3DnaJ heat shock protein family (Hsp40) member C3 | Dažnai (30–79%) | 1 ligoje |
| DNM1Ldynamin 1L | Dažnai (30–79%) | 1 ligoje |
Rodyti dar 67 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| EMILIN1elastin microfibril interfacer 1 | Dažnai (30–79%) | 1 ligoje |
| GBA2glucosylceramidase beta 2 | Dažnai (30–79%) | 1 ligoje |
| GJB1gap junction protein beta 1 | Dažnai (30–79%) | 1 ligoje |
| IFRD1interferon related developmental regulator 1 | Dažnai (30–79%) | 1 ligoje |
| KIF1Akinesin family member 1A | Dažnai (30–79%) | 2 ligose |
| MPZmyelin protein zero | Dažnai (30–79%) | 1 ligoje |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Dažnai (30–79%) | 1 ligoje |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Dažnai (30–79%) | 2 ligose |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Dažnai (30–79%) | 1 ligoje |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Dažnai (30–79%) | 1 ligoje |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Dažnai (30–79%) | 2 ligose |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Dažnai (30–79%) | 2 ligose |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Dažnai (30–79%) | 2 ligose |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Dažnai (30–79%) | 1 ligoje |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Dažnai (30–79%) | 2 ligose |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Dažnai (30–79%) | 1 ligoje |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Dažnai (30–79%) | 2 ligose |
| OPA1OPA1 mitochondrial dynamin like GTPase | Dažnai (30–79%) | 2 ligose |
| PEX6peroxisomal biogenesis factor 6 | Dažnai (30–79%) | 1 ligoje |
| PLA2G6phospholipase A2 group VI | Dažnai (30–79%) | 1 ligoje |
| PMP22peripheral myelin protein 22 | Dažnai (30–79%) | 2 ligose |
| PPIBpeptidylprolyl isomerase B | Dažnai (30–79%) | 1 ligoje |
| RFC1replication factor C subunit 1 | Dažnai (30–79%) | 1 ligoje |
| SACSsacsin molecular chaperone | Dažnai (30–79%) | 1 ligoje |
| SCO2synthesis of cytochrome C oxidase 2 | Dažnai (30–79%) | 1 ligoje |
| SLC25A46solute carrier family 25 member 46 | Dažnai (30–79%) | 1 ligoje |
| TDP1tyrosyl-DNA phosphodiesterase 1 | Dažnai (30–79%) | 1 ligoje |
| UCHL1ubiquitin C-terminal hydrolase L1 | Dažnai (30–79%) | 1 ligoje |
| VCPvalosin containing protein | Dažnai (30–79%) | 1 ligoje |
| VPS13Dvacuolar protein sorting 13 homolog D | Dažnai (30–79%) | 1 ligoje |
| VPS41VPS41 subunit of HOPS complex | Dažnai (30–79%) | 1 ligoje |
| VRK1VRK serine/threonine kinase 1 | Dažnai (30–79%) | 1 ligoje |
| AHCYadenosylhomocysteinase | Kartais (5–29%) | 1 ligoje |
| B2Mbeta-2-microglobulin | Kartais (5–29%) | 1 ligoje |
| GBA1glucosylceramidase beta 1 | Kartais (5–29%) | 1 ligoje |
| KIF5Akinesin family member 5A | Kartais (5–29%) | 1 ligoje |
| MRE11MRE11 double strand break repair nuclease | Kartais (5–29%) | 1 ligoje |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Kartais (5–29%) | 1 ligoje |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Kartais (5–29%) | 1 ligoje |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Kartais (5–29%) | 1 ligoje |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Kartais (5–29%) | 1 ligoje |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Kartais (5–29%) | 1 ligoje |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Kartais (5–29%) | 1 ligoje |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Kartais (5–29%) | 1 ligoje |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Kartais (5–29%) | 1 ligoje |
| PNKPpolynucleotide kinase 3'-phosphatase | Kartais (5–29%) | 1 ligoje |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | Kartais (5–29%) | 2 ligose |
| RNASEH1ribonuclease H1 | Kartais (5–29%) | 1 ligoje |
| RRM1ribonucleotide reductase catalytic subunit M1 | Kartais (5–29%) | 1 ligoje |
| SCARB2scavenger receptor class B member 2 | Kartais (5–29%) | 1 ligoje |
| SLC30A10solute carrier family 30 member 10 | Kartais (5–29%) | 1 ligoje |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Retai (1–4 %) | 1 ligoje |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Retai (1–4 %) | 1 ligoje |
| ABHD12abhydrolase domain containing 12, lysophospholipase | Neužfiksuota | 1 ligoje |
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Neužfiksuota | 1 ligoje |
| FDX2ferredoxin 2 | Neužfiksuota | 1 ligoje |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Neužfiksuota | 1 ligoje |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Neužfiksuota | 1 ligoje |
| MPV17mitochondrial inner membrane protein MPV17 | Neužfiksuota | 1 ligoje |
| NEFHneurofilament heavy chain | Neužfiksuota | 1 ligoje |
| PDYNprodynorphin | Neužfiksuota | 1 ligoje |
| PEX7peroxisomal biogenesis factor 7 | Neužfiksuota | 1 ligoje |
| PHYHphytanoyl-CoA 2-hydroxylase | Neužfiksuota | 1 ligoje |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Neužfiksuota | 1 ligoje |
| RPIAribose 5-phosphate isomerase A | Neužfiksuota | 1 ligoje |
| SCYL1SCY1 like pseudokinase 1 | Neužfiksuota | 1 ligoje |
| SLC52A2solute carrier family 52 member 2 | 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.
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AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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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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