AtlasAtlasDenne 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/spastic-ataxia.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Spastic ataxia, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test20 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.
- Cenani-Lenz Syndactyly SyndromeReads 1 of these genesLRP4About this report →
- TANC2-Related Neurodevelopmental DisorderReads 1 of these genesTANC2About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesHTRA1About this report →
- Inherited Neurodegenerative DisordersReads 10 of these genesCAPN1TUBA4AKIF1CTBCEDARS2GDAP2About this report →
Show 16 more reports
- TubulinopathiesReads 1 of these genesTUBB3About this report →
- Congenital Myasthenic SyndromeReads 2 of these genesLRP4VAMP1About this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesTUBB3About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesCAPN1KIF1CSPG7About this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesGLRX5About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesAFG3L2CACNA1GAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesAFG3L2About this report →
- Methylmalonic & Propionic AcidemiaReads 1 of these genesMMADHCAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesGDAP2SACSAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesTUBB3About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesMMADHCAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesTUBA4AAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesATP5F1AAFG3L2About this report →
- Female InfertilityReads 1 of these genesTUBA4AAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesDARS2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesPRDM8About this report →
Læs de gener, der er knyttet til Spastic ataxia, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test21 gener knyttet til Spastic ataxia
Ændringer i disse gener forårsager sjældne tilstande, hvor Spastic ataxia 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 |
|---|---|---|
| CAPN1calpain 1 | Altid | I 1 tilstand |
| MMADHCmetabolism of cobalamin associated D | Altid | I 2 tilstande |
| TUBA4Atubulin alpha 4a | Altid | I 1 tilstand |
| KIF1Ckinesin family member 1C | Meget ofte (80–99 %) | I 2 tilstande |
| MARS2methionyl-tRNA synthetase 2, mitochondrial | Meget ofte (80–99 %) | I 2 tilstande |
| TBCEtubulin folding cofactor E | Meget ofte (80–99 %) | I 1 tilstand |
| ATP5F1AATP synthase F1 subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| GDAP2ganglioside induced differentiation associated protein 2 | Ofte (30–79 %) | I 1 tilstand |
| HTRA1HtrA serine peptidase 1 | Ofte (30–79 %) | I 1 tilstand |
| LRP4LDL receptor related protein 4 | Ofte (30–79 %) | I 1 tilstand |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Ofte (30–79 %) | I 1 tilstand |
| TANC2tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 | Ofte (30–79 %) | I 1 tilstand |
| TUBB3tubulin beta 3 class III | Ofte (30–79 %) | I 1 tilstand |
| VAMP1vesicle associated membrane protein 1 | Ofte (30–79 %) | I 2 tilstande |
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Ikke registreret | I 1 tilstand |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Ikke registreret | I 1 tilstand |
| GLRX5glutaredoxin 5 | Ikke registreret | I 1 tilstand |
| MTPAPmitochondrial poly(A) polymerase | Ikke registreret | I 1 tilstand |
| PRDM8PR/SET domain 8 | Ikke registreret | I 1 tilstand |
| SACSsacsin molecular chaperone | 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.
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.
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.
Gratis forsendelse · Resultater på 6–8 uger
