AtlasKiknek segítünkTudományunkTermékekEredmények
BejelentkezésKérdezzenSzekvenálja genomját↗
Tulajdonság
Back pain
An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the back.
Összefoglaló
AtlasKiknek segítünkTudományunkTermékekEredmények
BejelentkezésKérdezzenSzekvenálja genomját↗
Ez az oldal adatként
Adja hozzá a .json végződést az oldal címéhez, vagy kérjen application/json típust, hogy JSON-ként olvassa be.
library(jsonlite)
url <- "https://dantelabs.com/traits/back-pain.json"
page <- fromJSON(url)
page$trait$nameBack painHP:0003418
AtlasKiknek segítünkTudományunkTermékekEredmények
BejelentkezésKérdezzenSzekvenálja genomját↗
Olvassa el a(z) Back pain nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet81 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.
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- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Renal HypouricemiaReads 2 of these genesSLC22A12SLC2A9About this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 2 of these genesSMARCB1SMARCE1About this report →
Show 77 more reports
- OsteopetrosisReads 4 of these genesCLCN7PLEKHM1TCIRG1LRP5About this report →
- Hepatic Porphyria DisordersReads 3 of these genesHMBSPPOXCPOXAbout this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 3 of these genesCD46CFHCFIAbout this report →
- Kidney CancerReads 3 of these genesTP53VHLBAP1About this report →
- PorphyriaReads 3 of these genesHMBSPPOXCPOXAbout this report →
- NeurofibromatosisReads 2 of these genesNF2SMARCB1About this report →
- AlkaptonuriaReads 1 of these genesHGDAbout this report →
- BAP1 Tumour Predisposition SyndromeReads 1 of these genesBAP1About this report →
- CLCN7-Related Hypopigmentation, Organomegaly and Delayed Myelination (HOD)Reads 1 of these genesCLCN7About this report →
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- Von Hippel-Lindau DiseaseReads 1 of these genesVHLAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 2 of these genesLRP5SFRP4About this report →
- Urinary and Renal System TumourReads 3 of these genesTP53VHLBAP1About this report →
- Dilated CardiomyopathyReads 5 of these genesFHL1EMDFLNCLMNASYNE1About this report →
- Fanconi AnemiaReads 3 of these genesBRCA1BRCA2PALB2About this report →
- Age-Related Macular DegenerationReads 1 of these genesCFHAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesHTRA1About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 1 of these genesSUFUAbout this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1MATN3About this report →
- Coffin-Siris SyndromeReads 2 of these genesSMARCB1SMARCE1About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Hereditary Vascular MalformationsReads 1 of these genesRASA1About this report →
- MelanomaReads 1 of these genesCDKN2AAbout this report →
- Distal MyopathiesReads 2 of these genesVCPFLNCAbout this report →
- DNA Repair DiseaseReads 3 of these genesBRCA1BRCA2PALB2About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- VitreoretinopathyReads 2 of these genesCOL2A1LRP5About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFBAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- Malignant Endocrine NeoplasmReads 1 of these genesTP53About this report →
- PolycythemiaReads 1 of these genesVHLAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLMNACAPN3About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesPALB2About this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesVHLAbout this report →
- Congenital Disorders of GlycosylationReads 3 of these genesDLL3MESP2ALG8About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesTMEM43About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesTBX18About this report →
- Polycystic Kidney DiseaseReads 1 of these genesALG8About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Frontotemporal DementiaReads 1 of these genesVCPAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesFLNCAbout this report →
- Other Inborn Errors of ImmunityReads 4 of these genesKRASCD46CFHCFIAbout this report →
- Hypertrophic CardiomyopathyReads 2 of these genesKRASFLNCAbout this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesCFIAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesVCPLMNAAbout this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Ehlers-Danlos SyndromeReads 1 of these genesTNXBAbout this report →
- Noonan SyndromeReads 1 of these genesKRASAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesTRAF7About this report →
- Syndromic CraniosynostosisReads 1 of these genesSMOAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesVCPAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesFLI1About this report →
- Osteogenesis ImperfectaReads 1 of these genesLRP5About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesSUFUAbout this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesVCPSYNE1ABCD1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSYNE1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesVCPLMNAAbout this report →
- Intellectual DisabilityReads 2 of these genesSMAD4SMARCB1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesABCD1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesABCD1About this report →
Olvassa el a(z) Back pain nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet68 gén kapcsolódik ehhez: Back pain
Ezeknek a géneknek a változásai olyan ritka betegségeket okoznak, amelyekben előfordul a(z) Back pain. A tulajdonsággal rendelkező emberek többségének nincs ezek közül egyik betegsége sem, a listán szereplő gének pedig semmit nem mondanak el senki saját genomjáról.
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| FHL1four and a half LIM domains 1 | Mindig | 2 betegségben |
| RAB32RAB32, member RAS oncogene family | Mindig | 1 betegségben |
| TRAPPC2trafficking protein particle complex subunit 2 | Mindig | 2 betegségben |
| VCPvalosin containing protein | Mindig | 2 betegségben |
| ATP7BATPase copper transporting beta | Nagyon gyakran (80–99%) | 1 betegségben |
| BRCA1BRCA1 DNA repair associated | Nagyon gyakran (80–99%) | 1 betegségben |
| BRCA2BRCA2 DNA repair associated | Nagyon gyakran (80–99%) | 1 betegségben |
| CDKN2Acyclin dependent kinase inhibitor 2A | Nagyon gyakran (80–99%) | 1 betegségben |
| KRASKRas proto-oncogene, GTPase | Nagyon gyakran (80–99%) | 1 betegségben |
| PALB2partner and localizer of BRCA2 | Nagyon gyakran (80–99%) | 1 betegségben |
| PALLDpalladin, cytoskeletal associated protein | Nagyon gyakran (80–99%) | 1 betegségben |
| RABL3RAB, member of RAS oncogene family like 3 | Nagyon gyakran (80–99%) | 1 betegségben |
| SMAD4SMAD family member 4 | Nagyon gyakran (80–99%) | 1 betegségben |
| TP53tumor protein p53 | Nagyon gyakran (80–99%) | 1 betegségben |
| CLCN7Cl-/H+ antiporter 7 | Gyakran (30–79%) | 1 betegségben |
| DLL3delta like canonical Notch ligand 3 | Gyakran (30–79%) | 1 betegségben |
| EMDemerin | Gyakran (30–79%) | 1 betegségben |
| FLNCfilamin C | Gyakran (30–79%) | 1 betegségben |
| HGDhomogentisate 1,2-dioxygenase | Gyakran (30–79%) | 1 betegségben |
| HMBShydroxymethylbilane synthase | Gyakran (30–79%) | 1 betegségben |
| HTRA1HtrA serine peptidase 1 | Gyakran (30–79%) | 1 betegségben |
| LMNAlamin A/C | Gyakran (30–79%) | 2 betegségben |
| LMX1BLIM homeobox transcription factor 1 beta | Gyakran (30–79%) | 2 betegségben |
| MESP2mesoderm posterior bHLH transcription factor 2 | Gyakran (30–79%) | 1 betegségben |
| NKX3-2NK3 homeobox 2 | Gyakran (30–79%) | 1 betegségben |
| PLEKHM1pleckstrin homology and RUN domain containing M1 | Gyakran (30–79%) | 1 betegségben |
| POLR3GLRNA polymerase III subunit GL | Gyakran (30–79%) | 1 betegségben |
| PPOXprotoporphyrinogen oxidase | Gyakran (30–79%) | 1 betegségben |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Gyakran (30–79%) | 1 betegségben |
| SYNE2spectrin repeat containing nuclear envelope protein 2 | Gyakran (30–79%) | 1 betegségben |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Gyakran (30–79%) | 1 betegségben |
| TMEM43transmembrane protein 43 | Gyakran (30–79%) | 1 betegségben |
| TNXBtenascin XB | Gyakran (30–79%) | 1 betegségben |
| ABCD1ATP binding cassette subfamily D member 1 | Néha (5–29%) | 1 betegségben |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Néha (5–29%) | 1 betegségben |
| CCND1cyclin D1 | Néha (5–29%) | 1 betegségben |
| CD46CD46 molecule | Néha (5–29%) | 1 betegségben |
| CFHcomplement factor H | Néha (5–29%) | 1 betegségben |
| CFIcomplement factor I | Néha (5–29%) | 1 betegségben |
| COL2A1collagen type II alpha 1 chain | Néha (5–29%) | 1 betegségben |
További 28 gén megjelenítése
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| CPOXcoproporphyrinogen oxidase | Néha (5–29%) | 1 betegségben |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Néha (5–29%) | 1 betegségben |
| HELLPARHELLP associated long non-coding RNA | Néha (5–29%) | 1 betegségben |
| LRP5LDL receptor related protein 5 | Néha (5–29%) | 1 betegségben |
| PRKCSHPRKCSH beta subunit of glucosidase II | Néha (5–29%) | 2 betegségben |
| RASA1RAS p21 protein activator 1 | Néha (5–29%) | 1 betegségben |
| SEC63SEC63 protein translocation regulator | Néha (5–29%) | 1 betegségben |
| SFRP4secreted frizzled related protein 4 | Néha (5–29%) | 1 betegségben |
| SLC22A12solute carrier family 22 member 12 | Néha (5–29%) | 1 betegségben |
| SLC2A9solute carrier family 2 member 9 | Néha (5–29%) | 1 betegségben |
| TBX18T-box transcription factor 18 | Néha (5–29%) | 1 betegségben |
| VHLvon Hippel-Lindau tumor suppressor | Néha (5–29%) | 1 betegségben |
| AKT1AKT serine/threonine kinase 1 | Ritkán (1–4%) | 1 betegségben |
| BAP1BRCA1 associated deubiquitinase 1 | Ritkán (1–4%) | 1 betegségben |
| MATN3matrilin 3 | Ritkán (1–4%) | 1 betegségben |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Ritkán (1–4%) | 1 betegségben |
| PDGFBplatelet derived growth factor subunit B | Ritkán (1–4%) | 1 betegségben |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Ritkán (1–4%) | 1 betegségben |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Ritkán (1–4%) | 1 betegségben |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Ritkán (1–4%) | 1 betegségben |
| SMOsmoothened, frizzled class receptor | Ritkán (1–4%) | 1 betegségben |
| SPTBN1spectrin beta, non-erythrocytic 1 | Ritkán (1–4%) | 1 betegségben |
| SUFUSUFU negative regulator of hedgehog signaling | Ritkán (1–4%) | 1 betegségben |
| TERTtelomerase reverse transcriptase | Ritkán (1–4%) | 1 betegségben |
| TRAF7TNF receptor associated factor 7 | Ritkán (1–4%) | 1 betegségben |
| CAPN3calpain 3 | Nincs rögzítve | 1 betegségben |
| HLA-Bmajor histocompatibility complex, class I, B | Nincs rögzítve | 1 betegségben |
| VANGL1VANGL planar cell polarity protein 1 | Nincs rögzítve | 1 betegségben |
Az, hogy milyen gyakran fordul elő a gén valamelyik állapotával élő emberek körében (a leggyakoribb érték, ahogyan a Human Phenotype Ontology rögzíti). Ezek az oldalak tulajdonságokat és az azok mögött álló kutatásokat ismertetik; nem diagnózist jelentenek. A tünetekkel kapcsolatban orvoshoz vagy genetikai tanácsadóhoz érdemes fordulni.
Szűkebb tulajdonságok
Tágabb tulajdonságok
Forrás
- Human Phenotype Ontology, 2026-09-01 kiadás: a tulajdonság, a nevei, a definíciója és a hozzá kapcsolt gének. További információ: hpo.jax.org.
- Adatkiadás: 2026.10.19-9814e911.
AtlasKiknek segítünkTudományunkTermékekEredmények
BejelentkezésKérdezzenSzekvenálja genomját↗
From traits to your genome
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Ingyenes szállítás · Eredmények 6–8 hét alatt
