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Træk
Glucose in urine
Klinisk navn: Glycosuria
An increased concentration of glucose in the urine.
Resumé
- Også kaldet
- Glucosuria
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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/glycosuria.json"
page <- fromJSON(url)
page$trait$nameGlucose in urineHP:0003076
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Læs de gener, der er knyttet til Glucose in urine, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test44 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.
- Maturity-Onset Diabetes Of The YoungReads 12 of these genesABCC8HNF4AGCKINSKCNJ11PDX1About this report →
- Diabetes MellitusReads 14 of these genesABCC8HNF4ASLC2A2GCKINSKCNJ11About this report →
- Neonatal Diabetes MellitusReads 9 of these genesABCC8SLC2A2GCKINSKCNJ11PDX1About this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 4 of these genesGATMHNF4ASLC5A2EHHADHAbout this report →
Show 40 more reports
- Primary Mitochondrial DiseaseReads 12 of these genesNDUFAF6COA8TRMT5RRM2BCOX10COX15About this report →
- CystinosisReads 1 of these genesCTNSAbout this report →
- Glucose-Galactose MalabsorptionReads 1 of these genesSLC5A1About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- HyperinsulinismReads 3 of these genesABCC8GCKKCNJ11About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 3 of these genesETFAETFBETFDHAbout this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesCLCN5About this report →
- Hypercalcemia InfantileReads 1 of these genesSLC34A1About this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Leigh SyndromeReads 5 of these genesNDUFAF6COX10SCO2SURF1TACO1About this report →
- Cerebral Creatine Deficiency SyndromesReads 1 of these genesGATMAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 1 of these genesALDOBAbout this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC2A2GYS2About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- Hypertrophic CardiomyopathyReads 3 of these genesETFAETFBETFDHAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- GlomerulosclerosisReads 1 of these genesPAX2About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesLMNASCO2SURF1About this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 1 of these genesFAN1About this report →
- Focal Segmental GlomerulosclerosisReads 1 of these genesPAX2About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesPAX2About this report →
- Polycystic Kidney DiseaseReads 1 of these genesIFT140About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Severe Congenital NeutropeniaReads 1 of these genesWASAbout this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesSLC5A1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA6About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Autoimmune DiseaseReads 1 of these genesSTAT3About this report →
- Inherited ThrombocytopeniasReads 1 of these genesWASAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- DNA Repair DiseaseReads 1 of these genesFAN1About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Other Inborn Errors of ImmunityReads 2 of these genesWASSTAT3About this report →
- Lysosomal Storage DiseaseReads 1 of these genesCTNSAbout this report →
- Retinitis PigmentosaReads 1 of these genesIFT140About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesPIGAAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesPIGAAbout this report →
Læs de gener, der er knyttet til Glucose in urine, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test54 gener knyttet til Glucose in urine
Ændringer i disse gener forårsager sjældne tilstande, hvor Glucose in urine 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 |
|---|---|---|
| ABCC8ATP binding cassette subfamily C member 8 | Altid | I 3 tilstande |
| CTNScystinosin, lysosomal cystine transporter | Altid | I 3 tilstande |
| GATMglycine amidinotransferase | Altid | I 2 tilstande |
| HNF4Ahepatocyte nuclear factor 4 alpha | Altid | I 3 tilstande |
| IFT140intraflagellar transport 140 | Altid | I 1 tilstand |
| SLC2A2solute carrier family 2 member 2 | Altid | I 2 tilstande |
| SLC34A1solute carrier family 34 member 1 | Altid | I 2 tilstande |
| SLC5A2solute carrier family 5 member 2 | Altid | I 2 tilstande |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Altid | I 1 tilstand |
| WASWASP actin nucleation promoting factor | Altid | I 1 tilstand |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Meget ofte (80–99 %) | I 2 tilstande |
| GCKglucokinase | Meget ofte (80–99 %) | I 2 tilstande |
| INSinsulin | Meget ofte (80–99 %) | I 2 tilstande |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Meget ofte (80–99 %) | I 2 tilstande |
| LMNAlamin A/C | Meget ofte (80–99 %) | I 1 tilstand |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Meget ofte (80–99 %) | I 2 tilstande |
| PDX1pancreatic and duodenal homeobox 1 | Meget ofte (80–99 %) | I 2 tilstande |
| STAT3signal transducer and activator of transcription 3 | Meget ofte (80–99 %) | I 1 tilstand |
| APPL1adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 | Ofte (30–79 %) | I 1 tilstand |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| CELcarboxyl ester lipase | Ofte (30–79 %) | I 1 tilstand |
| COA8cytochrome c oxidase assembly factor 8 | Ofte (30–79 %) | I 1 tilstand |
| FAN1FANCD2 and FANCI associated nuclease 1 | Ofte (30–79 %) | I 1 tilstand |
| GYS2glycogen synthase 2 | Ofte (30–79 %) | I 1 tilstand |
| HNF1AHNF1 homeobox A | Ofte (30–79 %) | I 1 tilstand |
| HNF1BHNF1 homeobox B | Ofte (30–79 %) | I 1 tilstand |
| KLF11KLF transcription factor 11 | Ofte (30–79 %) | I 1 tilstand |
| NEUROD1neuronal differentiation 1 | Ofte (30–79 %) | I 1 tilstand |
| PAX4paired box 4 | Ofte (30–79 %) | I 1 tilstand |
| SLC16A12solute carrier family 16 member 12 | Ofte (30–79 %) | I 1 tilstand |
| TRMT5tRNA methyltransferase 5 | Ofte (30–79 %) | I 1 tilstand |
| PAX2paired box 2 | Nogle gange (5–29 %) | I 1 tilstand |
| PBX1PBX homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Nogle gange (5–29 %) | I 1 tilstand |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Sjældent (1–4%) | I 1 tilstand |
| ALDOBaldolase, fructose-bisphosphate B | Ikke registreret | I 1 tilstand |
| ATP7BATPase copper transporting beta | Ikke registreret | I 1 tilstand |
| CLCN5Cl-/H+ antiporter 5 | Ikke registreret | I 2 tilstande |
| COX10cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 | Ikke registreret | I 1 tilstand |
| COX15cytochrome c oxidase assembly factor COX15 | Ikke registreret | I 1 tilstand |
Vis 14 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| COX6B1cytochrome c oxidase subunit 6B1 | Ikke registreret | I 1 tilstand |
| ETFAelectron transfer flavoprotein subunit alpha | Ikke registreret | I 1 tilstand |
| ETFBelectron transfer flavoprotein subunit beta | Ikke registreret | I 1 tilstand |
| ETFDHelectron transfer flavoprotein dehydrogenase | Ikke registreret | I 1 tilstand |
| FASTKD2FASTK mitochondrial RNA regulator 2 | Ikke registreret | I 1 tilstand |
| GATA6GATA binding protein 6 | Ikke registreret | I 1 tilstand |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Ikke registreret | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Ikke registreret | I 1 tilstand |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Ikke registreret | I 1 tilstand |
| SCO1synthesis of cytochrome C oxidase 1 | Ikke registreret | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Ikke registreret | I 1 tilstand |
| SLC5A1solute carrier family 5 member 1 | Ikke registreret | I 1 tilstand |
| SURF1SURF1 cytochrome c oxidase assembly factor | Ikke registreret | I 1 tilstand |
| TACO1translational activator of cytochrome c oxidase I | 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 2026.10.17-8666dff2.
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Read the genes behind these traits in your own DNA.
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