AtlasTræk
Gonadoblastoma
The presence of a gonadoblastoma, a neoplasm of a gonad that consists of aggregates of germ cells and sex cord elements.
Resumé
AtlasShare this page
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/gonadoblastoma.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til Gonadoblastoma, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test23 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.
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 8 of these genesDHHDHX37GATA4MAP3K1NR5A1SRYAbout this report →
- Hypertrophic CardiomyopathyReads 8 of these genesDHHDHX37MAP3K1NR5A1SRYZFPM2About this report →
- 46,XX Differences of Sex DevelopmentReads 2 of these genesNR5A1SRYAbout this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
Show 19 more reports
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesCDKN1CIGF2About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesZFPM2About this report →
- Tetralogy of FallotReads 1 of these genesZFPM2About this report →
- Familial Atrial FibrillationReads 1 of these genesKCNQ1About this report →
- Short Qt SyndromeReads 1 of these genesKCNQ1About this report →
- Diabetes MellitusReads 2 of these genesGATA4PAX6About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR0B1About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesPAX6About this report →
- Kidney CancerReads 1 of these genesPAX6About this report →
- Long QT SyndromeReads 1 of these genesKCNQ1About this report →
- Urinary and Renal System TumourReads 1 of these genesPAX6About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA4About this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA4About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesNR0B1About this report →
- Female InfertilityReads 1 of these genesNR5A1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesWWOXAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesWWOXAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesWWOXAbout this report →
Læs de gener, der er knyttet til Gonadoblastoma, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test17 gener knyttet til Gonadoblastoma
Ændringer i disse gener forårsager sjældne tilstande, hvor Gonadoblastoma 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 |
|---|---|---|
| DHHdesert hedgehog signaling molecule | Ofte (30–79 %) | I 2 tilstande |
| DHX37DEAH-box helicase 37 | Ofte (30–79 %) | I 1 tilstand |
| GATA4GATA binding protein 4 | Ofte (30–79 %) | I 1 tilstand |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Ofte (30–79 %) | I 2 tilstande |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Ofte (30–79 %) | I 1 tilstand |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Ofte (30–79 %) | I 1 tilstand |
| SOX9SRY-box transcription factor 9 | Ofte (30–79 %) | I 2 tilstande |
| SRYsex determining region Y | Ofte (30–79 %) | I 3 tilstande |
| VAMP7vesicle associated membrane protein 7 | Ofte (30–79 %) | I 1 tilstand |
| WT1WT1 transcription factor | Ofte (30–79 %) | I 4 tilstande |
| WWOXWW domain containing oxidoreductase | Ofte (30–79 %) | I 1 tilstand |
| ZFPM2zinc finger protein, FOG family member 2 | Ofte (30–79 %) | I 1 tilstand |
| PAX6paired box 6 | Nogle gange (5–29 %) | I 1 tilstand |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Ikke registreret | I 1 tilstand |
| IGF2insulin like growth factor 2 | Ikke registreret | I 1 tilstand |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Ikke registreret | I 1 tilstand |
| KCNQ1OT1KCNQ1 opposite strand/antisense transcript 1 | 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.
Snævrere træk
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
