AtlasEgenskap
Liver cysts
Klinisk navn: Hepatic cysts
Sammendrag
- Kroppssystem
- Abnormality of the digestive system
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hepatic-cysts.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Liver cysts, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt 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.
- Polycystic Kidney DiseaseReads 10 of these genesALG8ALG5ALG9DNAJB11GANABIFT140About this report →
- Polycystic Liver Disease (1 and 2)Reads 3 of these genesALG8LRP5SEC63About this report →
- Tuberous SclerosisReads 2 of these genesTSC1TSC2About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
Show 16 more reports
- JAK1-Related Autoinflammation, Immune Dysregulation and EosinophiliaReads 1 of these genesJAK1About this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 4 of these genesNEK8TTC21BWDR19NPHP3About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 2 of these genesWDR19IFT122About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesLRP5About this report →
- Syndromic CraniosynostosisReads 2 of these genesWDR19IFT122About this report →
- Retinitis PigmentosaReads 3 of these genesCC2D2AIFT140OFD1About this report →
- Joubert Syndrome And Related DisordersReads 2 of these genesCC2D2AOFD1About this report →
- OsteopetrosisReads 1 of these genesLRP5About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesALG8ALG9About this report →
- VitreoretinopathyReads 1 of these genesLRP5About this report →
- Osteogenesis ImperfectaReads 1 of these genesLRP5About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesCC2D2AAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesALPK3About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesCC2D2AAbout this report →
Les genene knyttet til Liver cysts, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test26 gener knyttet til Liver cysts
Endringer i disse genene forårsaker sjeldne tilstander der Liver cysts forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ALG8ALG8 alpha-1,3-glucosyltransferase | Alltid | I 1 tilstand |
| ALPK3alpha kinase 3 | Alltid | I 1 tilstand |
| CC2D2Acoiled-coil and C2 domain containing 2A | Alltid | I 1 tilstand |
| CILK1ciliogenesis associated kinase 1 | Alltid | I 1 tilstand |
| JAK1Janus kinase 1 | Alltid | I 1 tilstand |
| ALG5ALG5 dolichyl-phosphate beta-glucosyltransferase | Svært ofte (80–99 %) | I 1 tilstand |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Svært ofte (80–99 %) | I 2 tilstander |
| BICC1BicC family RNA binding protein 1 | Svært ofte (80–99 %) | I 1 tilstand |
| DNAJB11DnaJ heat shock protein family (Hsp40) member B11 | Svært ofte (80–99 %) | I 2 tilstander |
| GANABglucosidase II alpha subunit | Svært ofte (80–99 %) | I 2 tilstander |
| IFT140intraflagellar transport 140 | Svært ofte (80–99 %) | I 2 tilstander |
| NEK8NIMA related kinase 8 | Svært ofte (80–99 %) | I 4 tilstander |
| PKD1polycystin 1, transient receptor potential channel interacting | Svært ofte (80–99 %) | I 2 tilstander |
| PKD2polycystin 2, transient receptor potential cation channel | Svært ofte (80–99 %) | I 2 tilstander |
| EXTL3exostosin like glycosyltransferase 3 | Ofte (30–79 %) | I 1 tilstand |
| LRP5LDL receptor related protein 5 | Ofte (30–79 %) | I 1 tilstand |
| TTC21Btetratricopeptide repeat domain 21B | Ofte (30–79 %) | I 1 tilstand |
| WDR19WD repeat domain 19 | Ofte (30–79 %) | I 2 tilstander |
| IFNGinterferon gamma | Noen ganger (5–29 %) | I 1 tilstand |
| NPHP3nephrocystin 3 | Noen ganger (5–29 %) | I 2 tilstander |
| OFD1OFD1 centriole and centriolar satellite protein | Noen ganger (5–29 %) | I 1 tilstand |
| TSC1TSC complex subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TSC2TSC complex subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| IFT122intraflagellar transport 122 | Ikke registrert | I 1 tilstand |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Ikke registrert | I 1 tilstand |
| SEC63SEC63 protein translocation regulator | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
AtlasFrom traits to your genome
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