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Piirre
Glucose intolerance
Glucose intolerance (GI) can be defined as dysglycemia that comprises both prediabetes and diabetes. It includes the conditions of impaired fasting glucose (IFG) and impaired glucose tolerance (IGT) and diabetes mellitus (DM).
Yhteenveto
- Elimistön järjestelmä
- Laboratory abnormality
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Tämä sivu datana
Lisää sivun osoitteen perään .json tai pyydä application/json-muotoa, niin saat sivun JSON-muodossa.
library(jsonlite)
url <- "https://dantelabs.com/traits/glucose-intolerance.json"
page <- fromJSON(url)
page$trait$nameGlucose intoleranceHP:0001952
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Lue Glucose intolerance-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test60 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 genesABCC8APPL1CELGCKHNF1AHNF1BAbout this report →
- Diabetes MellitusReads 14 of these genesABCC8APPL1CELGCKHNF1AHNF1BAbout this report →
- Neonatal Diabetes MellitusReads 7 of these genesABCC8GCKHNF1BINSKCNJ11NEUROD1About this report →
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
Show 56 more reports
- Gitelman SyndromeReads 1 of these genesSLC12A3About this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- MTX2-Related Mandibuloacral DysplasiaReads 1 of these genesMTX2About this report →
- PDX1-Related Pancreatic AgenesisReads 1 of these genesPDX1About this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- HyperinsulinismReads 3 of these genesABCC8GCKKCNJ11About this report →
- LipodystrophyReads 3 of these genesLMNACAV1ZMPSTE24About this report →
- HemochromatosisReads 2 of these genesHFESLC40A1About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3R1About this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesAIPAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A4About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- HypertriglyceridemiaReads 1 of these genesAPOA5About this report →
- Wolfram Syndrome & WFS1 SpectrumReads 1 of these genesWFS1About this report →
- Primary Mitochondrial DiseaseReads 7 of these genesTRMT5GUK1POLGPOLG2RRM2BSLC25A4About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesARMC5About this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 1 of these genesHNF4AAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- Bartter DiseaseReads 1 of these genesCLCNKBAbout this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesCAV1About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesSLC25A4About this report →
- Hypodontia and AnodontiaReads 1 of these genesLRP6About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesSIM1About this report →
- Hepatic Porphyria DisordersReads 1 of these genesALAS2About this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesALAS2About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesPAX6About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesATMAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Kidney CancerReads 1 of these genesPAX6About this report →
- PorphyriaReads 1 of these genesALAS2About this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 1 of these genesPIK3R1About this report →
- Urinary and Renal System TumourReads 1 of these genesPAX6About this report →
- HyperlipidemiaReads 1 of these genesAPOA5About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Female InfertilityReads 2 of these genesTWNKATMAbout this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesWT1About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesIFT172About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesWFS1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesLMNAPOLGRRM2BAbout this report →
- Thyroid CancerReads 1 of these genesGNASAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesPOLGTWNKATMAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Other Inborn Errors of ImmunityReads 2 of these genesATMPIK3R1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTWNKAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesNSD1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Retinitis PigmentosaReads 1 of these genesIFT172About this report →
- Hearing Loss and DeafnessReads 1 of these genesWFS1About this report →
Lue Glucose intolerance-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test51 geeniä, jotka liittyvät piirteeseen Glucose intolerance
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Glucose intolerance esiintyy. Useimmilla, joilla on tämä piirre, ei ole mitään näistä sairauksista, eikä tämän listan geeni kerro mitään kenenkään omasta genomista.
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| LMNAlamin A/C | Aina | 1 sairaudessa |
| ABCC8ATP binding cassette subfamily C member 8 | Usein (30–79%) | 1 sairaudessa |
| APPL1adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 | Usein (30–79%) | 1 sairaudessa |
| ARMC5armadillo repeat containing 5 | Usein (30–79%) | 1 sairaudessa |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Usein (30–79%) | 1 sairaudessa |
| CELcarboxyl ester lipase | Usein (30–79%) | 1 sairaudessa |
| ESR1estrogen receptor 1 | Usein (30–79%) | 2 sairaudessa |
| GCKglucokinase | Usein (30–79%) | 1 sairaudessa |
| GNASGNAS complex locus | Usein (30–79%) | 1 sairaudessa |
| HNF1AHNF1 homeobox A | Usein (30–79%) | 1 sairaudessa |
| HNF1BHNF1 homeobox B | Usein (30–79%) | 1 sairaudessa |
| HNF4Ahepatocyte nuclear factor 4 alpha | Usein (30–79%) | 1 sairaudessa |
| INSinsulin | Usein (30–79%) | 1 sairaudessa |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Usein (30–79%) | 1 sairaudessa |
| KDM1Alysine demethylase 1A | Usein (30–79%) | 1 sairaudessa |
| KLF11KLF transcription factor 11 | Usein (30–79%) | 1 sairaudessa |
| NEUROD1neuronal differentiation 1 | Usein (30–79%) | 1 sairaudessa |
| PAX4paired box 4 | Usein (30–79%) | 1 sairaudessa |
| PDX1pancreatic and duodenal homeobox 1 | Usein (30–79%) | 1 sairaudessa |
| TRMT5tRNA methyltransferase 5 | Usein (30–79%) | 1 sairaudessa |
| WFS1wolframin ER transmembrane glycoprotein | Usein (30–79%) | 1 sairaudessa |
| ALAS25'-aminolevulinate synthase 2 | Joskus (5–29%) | 1 sairaudessa |
| CLCNKBchloride voltage-gated channel Kb | Joskus (5–29%) | 1 sairaudessa |
| GUK1guanylate kinase 1 | Joskus (5–29%) | 1 sairaudessa |
| IFT172intraflagellar transport 172 | Joskus (5–29%) | 1 sairaudessa |
| MTX2metaxin 2 | Joskus (5–29%) | 1 sairaudessa |
| POLGDNA polymerase gamma, catalytic subunit | Joskus (5–29%) | 1 sairaudessa |
| POLG2DNA polymerase gamma 2, accessory subunit | Joskus (5–29%) | 2 sairaudessa |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Joskus (5–29%) | 1 sairaudessa |
| SIM1SIM bHLH transcription factor 1 | Joskus (5–29%) | 1 sairaudessa |
| SLC12A3solute carrier family 12 member 3 | Joskus (5–29%) | 1 sairaudessa |
| SLC25A4solute carrier family 25 member 4 | Joskus (5–29%) | 1 sairaudessa |
| TWNKtwinkle mtDNA helicase | Joskus (5–29%) | 1 sairaudessa |
| AIPAHR interacting HSP90 co-chaperone | Ei kirjattu | 1 sairaudessa |
| APOA5apolipoprotein A5 | Ei kirjattu | 1 sairaudessa |
| ATMATM serine/threonine kinase | Ei kirjattu | 1 sairaudessa |
| BMP2bone morphogenetic protein 2 | Ei kirjattu | 1 sairaudessa |
| CAV1caveolin 1 | Ei kirjattu | 1 sairaudessa |
| ELNelastin | Ei kirjattu | 1 sairaudessa |
| HFEhomeostatic iron regulator | Ei kirjattu | 1 sairaudessa |
Näytä 11 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| LRP6LDL receptor related protein 6 | Ei kirjattu | 1 sairaudessa |
| MLXIPLMLX interacting protein like | Ei kirjattu | 1 sairaudessa |
| NSD1nuclear receptor binding SET domain protein 1 | Ei kirjattu | 1 sairaudessa |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Ei kirjattu | 1 sairaudessa |
| PAX6paired box 6 | Ei kirjattu | 1 sairaudessa |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Ei kirjattu | 1 sairaudessa |
| SLC40A1solute carrier family 40 member 1 | Ei kirjattu | 1 sairaudessa |
| USP8ubiquitin specific peptidase 8 | Ei kirjattu | 1 sairaudessa |
| WT1WT1 transcription factor | Ei kirjattu | 1 sairaudessa |
| ZBTB20zinc finger and BTB domain containing 20 | Ei kirjattu | 1 sairaudessa |
| ZMPSTE24zinc metallopeptidase STE24 | Ei kirjattu | 1 sairaudessa |
Kuinka usein ilmiö esiintyy ihmisillä, joilla on jokin geenin sairauksista, niin kuin Human Phenotype Ontology sen kirjaa. Nämä sivut kuvaavat piirteitä ja niiden taustalla olevaa tutkimusta, eivätkä ne ole diagnoosi. Oireista kannattaa kysyä lääkäriltä tai geneettiseltä neuvojalta.
Tarkemmat piirteet
Laajemmat piirteet
Mistä tämä tieto tulee
- Human Phenotype Ontology, julkaisu 2026-09-01: piirre, sen nimet, määritelmä ja siihen liitetyt geenit. Lue lisää osoitteesta hpo.jax.org.
- Tietojulkaisu 2026.10.18-8b139e39.
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
From 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.
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