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Požymis
Glucose in urine
Klinikinis pavadinimas: Glycosuria
An increased concentration of glucose in the urine.
Santrauka
- Taip pat vadinama
- Glucosuria
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/glycosuria.json"
page <- fromJSON(url)
page$trait$nameGlucose in urineHP:0003076
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Glucose in urine, ir kitą jūsų genomo dalį.
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Įsigyti savo 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 →
Vienu tyrimu sužinokite genus, susijusius su Glucose in urine, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test54 genų susiję su Glucose in urine
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Glucose in urine. 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 |
|---|---|---|
| ABCC8ATP binding cassette subfamily C member 8 | Visada | 3 ligose |
| CTNScystinosin, lysosomal cystine transporter | Visada | 3 ligose |
| GATMglycine amidinotransferase | Visada | 2 ligose |
| HNF4Ahepatocyte nuclear factor 4 alpha | Visada | 3 ligose |
| IFT140intraflagellar transport 140 | Visada | 1 ligoje |
| SLC2A2solute carrier family 2 member 2 | Visada | 2 ligose |
| SLC34A1solute carrier family 34 member 1 | Visada | 2 ligose |
| SLC5A2solute carrier family 5 member 2 | Visada | 2 ligose |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Visada | 1 ligoje |
| WASWASP actin nucleation promoting factor | Visada | 1 ligoje |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Labai dažnai (80–99%) | 2 ligose |
| GCKglucokinase | Labai dažnai (80–99%) | 2 ligose |
| INSinsulin | Labai dažnai (80–99%) | 2 ligose |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Labai dažnai (80–99%) | 2 ligose |
| LMNAlamin A/C | Labai dažnai (80–99%) | 1 ligoje |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Labai dažnai (80–99%) | 2 ligose |
| PDX1pancreatic and duodenal homeobox 1 | Labai dažnai (80–99%) | 2 ligose |
| STAT3signal transducer and activator of transcription 3 | Labai dažnai (80–99%) | 1 ligoje |
| APPL1adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 | Dažnai (30–79%) | 1 ligoje |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Dažnai (30–79%) | 1 ligoje |
| CELcarboxyl ester lipase | Dažnai (30–79%) | 1 ligoje |
| COA8cytochrome c oxidase assembly factor 8 | Dažnai (30–79%) | 1 ligoje |
| FAN1FANCD2 and FANCI associated nuclease 1 | Dažnai (30–79%) | 1 ligoje |
| GYS2glycogen synthase 2 | Dažnai (30–79%) | 1 ligoje |
| HNF1AHNF1 homeobox A | Dažnai (30–79%) | 1 ligoje |
| HNF1BHNF1 homeobox B | Dažnai (30–79%) | 1 ligoje |
| KLF11KLF transcription factor 11 | Dažnai (30–79%) | 1 ligoje |
| NEUROD1neuronal differentiation 1 | Dažnai (30–79%) | 1 ligoje |
| PAX4paired box 4 | Dažnai (30–79%) | 1 ligoje |
| SLC16A12solute carrier family 16 member 12 | Dažnai (30–79%) | 1 ligoje |
| TRMT5tRNA methyltransferase 5 | Dažnai (30–79%) | 1 ligoje |
| PAX2paired box 2 | Kartais (5–29%) | 1 ligoje |
| PBX1PBX homeobox 1 | Kartais (5–29%) | 1 ligoje |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Kartais (5–29%) | 1 ligoje |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Retai (1–4 %) | 1 ligoje |
| ALDOBaldolase, fructose-bisphosphate B | Neužfiksuota | 1 ligoje |
| ATP7BATPase copper transporting beta | Neužfiksuota | 1 ligoje |
| CLCN5Cl-/H+ antiporter 5 | Neužfiksuota | 2 ligose |
| COX10cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 | Neužfiksuota | 1 ligoje |
| COX15cytochrome c oxidase assembly factor COX15 | Neužfiksuota | 1 ligoje |
Rodyti dar 14 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| COX6B1cytochrome c oxidase subunit 6B1 | Neužfiksuota | 1 ligoje |
| ETFAelectron transfer flavoprotein subunit alpha | Neužfiksuota | 1 ligoje |
| ETFBelectron transfer flavoprotein subunit beta | Neužfiksuota | 1 ligoje |
| ETFDHelectron transfer flavoprotein dehydrogenase | Neužfiksuota | 1 ligoje |
| FASTKD2FASTK mitochondrial RNA regulator 2 | Neužfiksuota | 1 ligoje |
| GATA6GATA binding protein 6 | Neužfiksuota | 1 ligoje |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Neužfiksuota | 1 ligoje |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Neužfiksuota | 1 ligoje |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Neužfiksuota | 1 ligoje |
| SCO1synthesis of cytochrome C oxidase 1 | Neužfiksuota | 1 ligoje |
| SCO2synthesis of cytochrome C oxidase 2 | Neužfiksuota | 1 ligoje |
| SLC5A1solute carrier family 5 member 1 | Neužfiksuota | 1 ligoje |
| SURF1SURF1 cytochrome c oxidase assembly factor | Neužfiksuota | 1 ligoje |
| TACO1translational activator of cytochrome c oxidase I | 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 2026.10.17-8666dff2.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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