AtlasAtlasŠi puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/axonal-degeneration.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Axonal degeneration, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test21 condition report reads 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.
- Charcot-Marie-Tooth DiseaseReads 10 of these genesREEP1LMNADNM2GDAP1GJB1IGHMBP2About this report →
- Cerebrotendinous XanthomatosisReads 1 of these genesCYP27A1About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 13 of these genesREEP1LMNACYP27A1DNM2GDAP1GJB1About this report →
Show 17 more reports
- Hereditary AngioedemaReads 1 of these genesSERPING1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 4 of these genesFLVCR1CYP27A1CTDP1SETXAbout this report →
- Inherited Neurodegenerative DisordersReads 9 of these genesREEP1ABCD1FLVCR1CYP27A1APTXCTDP1About this report →
- DNA Repair DiseaseReads 3 of these genesERCC6APTXSETXAbout this report →
- Spinal Muscular AtrophyReads 2 of these genesREEP1IGHMBP2About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesNAGAAbout this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesREEP1ABCD1TFGAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLAMA2LMNAAbout this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesCYP27A1NAGAAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesABCD1CYP27A1About this report →
- Congenital MyopathiesReads 1 of these genesDNM2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesSETXAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesLAMA2About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Retinitis PigmentosaReads 1 of these genesFLVCR1About this report →
Vienu tyrimu sužinokite genus, susijusius su Axonal degeneration, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test23 genų susiję su Axonal degeneration
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Axonal degeneration. 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 |
|---|---|---|
| LAMA2laminin subunit alpha 2 | Visada | 1 ligoje |
| REEP1receptor accessory protein 1 | Visada | 1 ligoje |
| SERPING1serpin family G member 1 | Visada | 1 ligoje |
| SLC25A21solute carrier family 25 member 21 | Visada | 1 ligoje |
| ABCD1ATP binding cassette subfamily D member 1 | Labai dažnai (80–99%) | 1 ligoje |
| LMNAlamin A/C | Labai dažnai (80–99%) | 1 ligoje |
| TXN2thioredoxin 2 | Labai dažnai (80–99%) | 2 ligose |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Dažnai (30–79%) | 1 ligoje |
| FLVCR1FLVCR choline and heme transporter 1 | Dažnai (30–79%) | 1 ligoje |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Kartais (5–29%) | 1 ligoje |
| APTXaprataxin | Neužfiksuota | 1 ligoje |
| CTDP1CTD phosphatase 1 | Neužfiksuota | 1 ligoje |
| DNM2dynamin 2 | Neužfiksuota | 1 ligoje |
| GDAP1ganglioside induced differentiation associated protein 1 | Neužfiksuota | 1 ligoje |
| GJB1gap junction protein beta 1 | Neužfiksuota | 1 ligoje |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Neužfiksuota | 2 ligose |
| LRSAM1leucine rich repeat and sterile alpha motif containing 1 | Neužfiksuota | 1 ligoje |
| NAGAalpha-N-acetylgalactosaminidase | Neužfiksuota | 1 ligoje |
| SEPTIN9septin 9 | Neužfiksuota | 1 ligoje |
| SETXsenataxin | Neužfiksuota | 1 ligoje |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Neužfiksuota | 1 ligoje |
| TFGtrafficking from ER to golgi regulator | Neužfiksuota | 1 ligoje |
| TRIM2tripartite motif containing 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.
Platesni požymiai
Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
AtlasFrom 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 810+ physician-ready reports.
Nemokamas pristatymas · Rezultatai per 6–8 savaites
