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Požymis
Cancer of early nerve cells
Klinikinis pavadinimas: Neuroblastoma
Neuroblastoma is a solid tumor that originate in neural crest cells of the sympathetic nervous system. Most neuroblastomas originate in the abdomen, and most abdominal neuroblastomas originate in the adrenal gland. Neuroblastomas can also originate in the thorax, usually in the posterior mediastinum.
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Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/neuroblastoma.json"
page <- fromJSON(url)
page$trait$nameCancer of early nerve cellsHP:0003006
AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Cancer of early nerve cells, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test52 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.
- Lynch SyndromeReads 5 of these genesEPCAMMLH1MSH2MSH6PMS2About this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 2 of these genesALKPHOX2BAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesPHOX2BRETAbout this report →
- Colorectal Cancer & PolyposisReads 3 of these genesMUTYHPOLD1POLEAbout this report →
Show 48 more reports
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesATMCHEK2PALB2About this report →
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- MDPL SyndromeReads 1 of these genesPOLD1About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- DNA Repair DiseaseReads 6 of these genesBRCA2MLH1MSH2MSH6PALB2PMS2About this report →
- Noonan SyndromeReads 4 of these genesBRAFKRASPTPN11RAF1About this report →
- Malignant Endocrine NeoplasmReads 2 of these genesRETSDHBAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 1 of these genesBRCA2About this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Hypertrophic CardiomyopathyReads 5 of these genesBRAFKRASPTPN11RAF1NSD1About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 2 of these genesRETSDHBAbout this report →
- Marfan Like SyndromesReads 2 of these genesSKITGFBR2About this report →
- Urinary and Renal System TumourReads 2 of these genesRETSDHBAbout this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesREREAbout this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesSDHBAbout this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Fanconi AnemiaReads 2 of these genesBRCA2PALB2About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesBRD4About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR2About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesRUNX1About this report →
- Waardenburg SyndromeReads 1 of these genesEDN3About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Kidney CancerReads 1 of these genesSDHBAbout this report →
- Dilated CardiomyopathyReads 2 of these genesPRDM16RAF1About this report →
- Aortic AneurysmReads 1 of these genesTGFBR2About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesEPCAMAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesAPC2About this report →
- Syndromic CraniosynostosisReads 1 of these genesSKIAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesATMKRASPOLD1About this report →
- Thyroid CancerReads 1 of these genesRETAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesRUNX1About this report →
- Female InfertilityReads 1 of these genesATMAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesHACE1About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesHACE1ATMAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesHACE1About this report →
- Intellectual DisabilityReads 1 of these genesBRD4About this report →
Vienu tyrimu sužinokite genus, susijusius su Cancer of early nerve cells, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test60 genų susiję su Cancer of early nerve cells
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Cancer of early nerve cells. 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 |
|---|---|---|
| MYCNMYCN proto-oncogene, bHLH transcription factor | Visada | 2 ligose |
| ALKALK receptor tyrosine kinase | Labai dažnai (80–99%) | 1 ligoje |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Labai dažnai (80–99%) | 1 ligoje |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Labai dažnai (80–99%) | 1 ligoje |
| LMO1LIM domain only 1 | Labai dažnai (80–99%) | 1 ligoje |
| PHOX2Bpaired like homeobox 2B | Labai dažnai (80–99%) | 5 ligose |
| BRD4bromodomain containing 4 | Dažnai (30–79%) | 1 ligoje |
| NUTM1NUT midline carcinoma family member 1 | Dažnai (30–79%) | 1 ligoje |
| ASCL1achaete-scute family bHLH transcription factor 1 | Kartais (5–29%) | 1 ligoje |
| ATMATM serine/threonine kinase | Kartais (5–29%) | 1 ligoje |
| BDNFbrain derived neurotrophic factor | Kartais (5–29%) | 1 ligoje |
| BMPR1Abone morphogenetic protein receptor type 1A | Kartais (5–29%) | 1 ligoje |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Kartais (5–29%) | 1 ligoje |
| BRCA2BRCA2 DNA repair associated | Kartais (5–29%) | 1 ligoje |
| CASZ1castor zinc finger 1 | Kartais (5–29%) | 1 ligoje |
| CHEK2checkpoint kinase 2 | Kartais (5–29%) | 1 ligoje |
| EDN3endothelin 3 | Kartais (5–29%) | 1 ligoje |
| EPCAMepithelial cell adhesion molecule | Kartais (5–29%) | 1 ligoje |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Kartais (5–29%) | 1 ligoje |
| GDNFglial cell derived neurotrophic factor | Kartais (5–29%) | 1 ligoje |
| GPC3glypican 3 | Kartais (5–29%) | 1 ligoje |
| GPC4glypican 4 | Kartais (5–29%) | 1 ligoje |
| HSPG2heparan sulfate proteoglycan 2 | Kartais (5–29%) | 1 ligoje |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Kartais (5–29%) | 1 ligoje |
| KRASKRas proto-oncogene, GTPase | Kartais (5–29%) | 1 ligoje |
| LBX1ladybird homeobox 1 | Kartais (5–29%) | 1 ligoje |
| LUZP1leucine zipper protein 1 | Kartais (5–29%) | 1 ligoje |
| MLH1mutL homolog 1 | Kartais (5–29%) | 2 ligose |
| MMP23Bmatrix metallopeptidase 23B | Kartais (5–29%) | 1 ligoje |
| MSH2mutS homolog 2 | Kartais (5–29%) | 1 ligoje |
| MSH6mutS homolog 6 | Kartais (5–29%) | 1 ligoje |
| MUTYHmutY DNA glycosylase | Kartais (5–29%) | 1 ligoje |
| MYO1Hmyosin IH | Kartais (5–29%) | 1 ligoje |
| NPATnuclear protein, coactivator of histone transcription | Kartais (5–29%) | 1 ligoje |
| PALB2partner and localizer of BRCA2 | Kartais (5–29%) | 1 ligoje |
| PDPNpodoplanin | Kartais (5–29%) | 1 ligoje |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Kartais (5–29%) | 1 ligoje |
| PMS1PMS1 homolog 1, mismatch repair system component | Kartais (5–29%) | 1 ligoje |
| PMS2PMS1 homolog 2, mismatch repair system component | Kartais (5–29%) | 1 ligoje |
| POLD1DNA polymerase delta 1, catalytic subunit | Kartais (5–29%) | 1 ligoje |
Rodyti dar 20 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| POLEDNA polymerase epsilon, catalytic subunit | Kartais (5–29%) | 1 ligoje |
| PRDM16PR/SET domain 16 | Kartais (5–29%) | 1 ligoje |
| PRKCZprotein kinase C zeta | Kartais (5–29%) | 1 ligoje |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Kartais (5–29%) | 1 ligoje |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Kartais (5–29%) | 1 ligoje |
| REREarginine-glutamic acid dipeptide repeats | Kartais (5–29%) | 1 ligoje |
| RETret proto-oncogene | Kartais (5–29%) | 1 ligoje |
| RPS20ribosomal protein S20 | Kartais (5–29%) | 1 ligoje |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Kartais (5–29%) | 1 ligoje |
| SEMA4Asemaphorin 4A | Kartais (5–29%) | 1 ligoje |
| SKISKI proto-oncogene | Kartais (5–29%) | 1 ligoje |
| SPENspen family transcriptional repressor | Kartais (5–29%) | 1 ligoje |
| TGFBR2transforming growth factor beta receptor 2 | Kartais (5–29%) | 1 ligoje |
| UBE4Bubiquitination factor E4B | Kartais (5–29%) | 1 ligoje |
| YY1YY1 transcription factor | Kartais (5–29%) | 1 ligoje |
| APC2APC regulator of Wnt signaling pathway 2 | Retai (1–4 %) | 1 ligoje |
| NF1neurofibromin 1 | Retai (1–4 %) | 1 ligoje |
| NSD1nuclear receptor binding SET domain protein 1 | Retai (1–4 %) | 1 ligoje |
| KIF1Bkinesin family member 1B | Neužfiksuota | 1 ligoje |
| RUNX1RUNX family transcription factor 1 | 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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- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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