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PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Flushing
Recurrent episodes of redness of the skin together with a sensation of warmth or burning of the affected areas of skin.
Santrauka
- Kūno sistema
- Abnormality of the integument
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/flushing.json"
page <- fromJSON(url)
page$trait$nameFlushingHP:0031284
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Flushing, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test46 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.
- Hereditary Pheochromocytoma and ParagangliomaReads 9 of these genesMAXRETSDHASDHAF2SDHBSDHCAbout this report →
- Malignant Endocrine NeoplasmReads 5 of these genesRETSDHASDHAF2SDHBTP53About this report →
- Urinary and Renal System TumourReads 6 of these genesRETSDHASDHAF2SDHBVHLTP53About this report →
- Hereditary Episodic AtaxiasReads 3 of these genesCACNA1ASCN2ASLC1A3About this report →
Show 42 more reports
- Hereditary Gastrointestinal Stromal TumourReads 3 of these genesSDHBSDHCKITAbout this report →
- Familial Hemiplegic MigraineReads 2 of these genesATP1A2CACNA1AAbout this report →
- Kidney CancerReads 3 of these genesSDHBVHLTP53About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 2 of these genesDNMT3ANSD1About this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- Hereditary Leiomyomatosis and Renal Cell CancerReads 1 of these genesFHAbout this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Von Hippel-Lindau DiseaseReads 1 of these genesVHLAbout this report →
- Epilepsy (Full Panel)Reads 12 of these genesATP1A2ATP1A3CACNA1AMDH2RHOBTB2SCN2AAbout this report →
- PolycythemiaReads 2 of these genesEPAS1VHLAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesRETAbout this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 1 of these genesHNF4AAbout this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Noonan SyndromeReads 2 of these genesCBLBRAFAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesRUNX1About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR3C1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesATP1A3CACNA1AAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesATP1A3SLC2A1About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesMAOAAbout this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF4AAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesATP1A3About this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesNSD1BRAFAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Congenital MyopathiesReads 1 of these genesRYR1About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesCBSAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesSCN9AAbout this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesAPC2About this report →
- Hearing Loss and DeafnessReads 2 of these genesCDH23USP48About this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesFHSDHASCN9AAbout this report →
- Intellectual DisabilityReads 3 of these genesASXL1SCN2AATRXAbout this report →
- Diabetes MellitusReads 1 of these genesHNF4AAbout this report →
- Thyroid CancerReads 1 of these genesRETAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesRUNX1About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesATP1A3CACNA1ASDHAAbout this report →
- Leigh SyndromeReads 1 of these genesSDHAAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTET2About this report →
Vienu tyrimu sužinokite genus, susijusius su Flushing, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test51 genas susijęs su Flushing
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Flushing. 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 |
|---|---|---|
| ADGRE2adhesion G protein-coupled receptor E2 | Visada | 1 ligoje |
| CBScystathionine beta-synthase | Visada | 1 ligoje |
| APC2APC regulator of Wnt signaling pathway 2 | Dažnai (30–79%) | 1 ligoje |
| ASXL1ASXL transcriptional regulator 1 | Dažnai (30–79%) | 2 ligose |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Dažnai (30–79%) | 1 ligoje |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Dažnai (30–79%) | 1 ligoje |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Dažnai (30–79%) | 1 ligoje |
| CBLCbl proto-oncogene | Dažnai (30–79%) | 1 ligoje |
| DLSTdihydrolipoamide S-succinyltransferase | Dažnai (30–79%) | 1 ligoje |
| DNMT3ADNA methyltransferase 3 alpha | Dažnai (30–79%) | 1 ligoje |
| EPAS1endothelial PAS domain protein 1 | Dažnai (30–79%) | 1 ligoje |
| FHfumarate hydratase | Dažnai (30–79%) | 1 ligoje |
| KIF1Bkinesin family member 1B | Dažnai (30–79%) | 1 ligoje |
| MAXMYC associated transcriptional regulator X | Dažnai (30–79%) | 1 ligoje |
| MDH2malate dehydrogenase 2 | Dažnai (30–79%) | 1 ligoje |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Dažnai (30–79%) | 1 ligoje |
| NF1neurofibromin 1 | Dažnai (30–79%) | 1 ligoje |
| NSD1nuclear receptor binding SET domain protein 1 | Dažnai (30–79%) | 1 ligoje |
| RETret proto-oncogene | Dažnai (30–79%) | 3 ligose |
| RHOBTB2Rho related BTB domain containing 2 | Dažnai (30–79%) | 1 ligoje |
| RUNX1RUNX family transcription factor 1 | Dažnai (30–79%) | 1 ligoje |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Dažnai (30–79%) | 1 ligoje |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Dažnai (30–79%) | 1 ligoje |
| SDHAF2succinate dehydrogenase complex assembly factor 2 | Dažnai (30–79%) | 1 ligoje |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Dažnai (30–79%) | 2 ligose |
| SDHCsuccinate dehydrogenase complex subunit C | Dažnai (30–79%) | 1 ligoje |
| SDHDsuccinate dehydrogenase complex subunit D | Dažnai (30–79%) | 2 ligose |
| SLC1A3solute carrier family 1 member 3 | Dažnai (30–79%) | 1 ligoje |
| SLC25A11solute carrier family 25 member 11 | Dažnai (30–79%) | 1 ligoje |
| SLC2A1solute carrier family 2 member 1 | Dažnai (30–79%) | 1 ligoje |
| SRSF2serine and arginine rich splicing factor 2 | Dažnai (30–79%) | 2 ligose |
| TET2tet methylcytosine dioxygenase 2 | Dažnai (30–79%) | 2 ligose |
| TMEM127transmembrane protein 127 | Dažnai (30–79%) | 1 ligoje |
| VHLvon Hippel-Lindau tumor suppressor | Dažnai (30–79%) | 2 ligose |
| ATRXATRX chromatin remodeler | Kartais (5–29%) | 1 ligoje |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Kartais (5–29%) | 1 ligoje |
| CDH23cadherin related 23 | Kartais (5–29%) | 1 ligoje |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Kartais (5–29%) | 1 ligoje |
| KITKIT proto-oncogene, receptor tyrosine kinase | Kartais (5–29%) | 2 ligose |
| NPRL2NPR2 like, GATOR1 complex subunit | Kartais (5–29%) | 1 ligoje |
Rodyti dar 11 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| NPRL3NPR3 like, GATOR1 complex subunit | Kartais (5–29%) | 1 ligoje |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Kartais (5–29%) | 1 ligoje |
| RYR1ryanodine receptor 1 | Kartais (5–29%) | 1 ligoje |
| SCN3Asodium voltage-gated channel alpha subunit 3 | Kartais (5–29%) | 1 ligoje |
| TP53tumor protein p53 | Kartais (5–29%) | 1 ligoje |
| USP48ubiquitin specific peptidase 48 | Kartais (5–29%) | 1 ligoje |
| USP8ubiquitin specific peptidase 8 | Kartais (5–29%) | 1 ligoje |
| MAOAmonoamine oxidase A | Retai (1–4 %) | 1 ligoje |
| HNF4Ahepatocyte nuclear factor 4 alpha | Neužfiksuota | 1 ligoje |
| HPGD15-hydroxyprostaglandin dehydrogenase | Neužfiksuota | 1 ligoje |
| SCN9Asodium voltage-gated channel alpha subunit 9 | 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.
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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 2026.10.18-8b139e39.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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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Nemokamas pristatymas · Rezultatai per 6–8 savaites
