AtlasTræk
B-cell lymphoma
A type of lymphoma that originates in B-cells.
Resumé
- Også kaldet
- B cell lymphoma
AtlasDenne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/b-cell-lymphoma.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til B-cell lymphoma, og resten af dit genom, med én test.
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Bestil min Genome Test20 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.
- Other Inborn Errors of ImmunityReads 17 of these genesITPR3MAGT1PTPRCRASGRP1ATMBCL10About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 3 of these genesCASP10FASFASLGAbout this report →
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
- DIAPH1-Related Microcephaly, Seizures and Cortical BlindnessReads 1 of these genesDIAPH1About this report →
Show 16 more reports
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3R1About this report →
- Autoimmune DiseaseReads 3 of these genesCASP10FASFASLGAbout this report →
- X-Linked Lymphoproliferative Disease and XMENReads 1 of these genesMAGT1About this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT6About this report →
- Severe Combined ImmunodeficiencyReads 2 of these genesPTPRCADAAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesATMAbout this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 1 of these genesPIK3R1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesDIAPH1About this report →
- DNA Repair DiseaseReads 1 of these genesNBNAbout this report →
- Female InfertilityReads 1 of these genesATMAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesITPR3About this report →
- Hearing Loss and DeafnessReads 1 of these genesDIAPH1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesITPR3About this report →
- Intellectual DisabilityReads 1 of these genesFOXP1About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesATMAbout this report →
Læs de gener, der er knyttet til B-cell lymphoma, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test24 gener knyttet til B-cell lymphoma
Ændringer i disse gener forårsager sjældne tilstande, hvor B-cell lymphoma ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Altid | I 1 tilstand |
| MAGT1magnesium transporter 1 | Altid | I 1 tilstand |
| NFATC2nuclear factor of activated T cells 2 | Altid | I 1 tilstand |
| PTPRCprotein tyrosine phosphatase receptor type C | Altid | I 1 tilstand |
| RASGRP1RAS guanyl releasing protein 1 | Altid | I 1 tilstand |
| ATMATM serine/threonine kinase | Meget ofte (80–99 %) | I 1 tilstand |
| BCL10BCL10 immune signaling adaptor | Meget ofte (80–99 %) | I 1 tilstand |
| BIRC3baculoviral IAP repeat containing 3 | Meget ofte (80–99 %) | I 1 tilstand |
| CCND1cyclin D1 | Meget ofte (80–99 %) | I 1 tilstand |
| FOXP1forkhead box P1 | Meget ofte (80–99 %) | I 1 tilstand |
| IGHimmunoglobulin heavy locus | Meget ofte (80–99 %) | I 2 tilstande |
| MALT1MALT1 paracaspase | Meget ofte (80–99 %) | I 1 tilstand |
| IKZF3IKAROS family zinc finger 3 | Ofte (30–79 %) | I 1 tilstand |
| ITKIL2 inducible T cell kinase | Ofte (30–79 %) | I 1 tilstand |
| SYKspleen associated tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| CASP10caspase 10 | Nogle gange (5–29 %) | I 1 tilstand |
| DIAPH1diaphanous related formin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| FASFas cell surface death receptor | Nogle gange (5–29 %) | I 1 tilstand |
| FASLGFas ligand | Nogle gange (5–29 %) | I 1 tilstand |
| FCHO1FCH and mu domain containing endocytic adaptor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| NBNnibrin | Nogle gange (5–29 %) | I 1 tilstand |
| STAT6signal transducer and activator of transcription 6 | Nogle gange (5–29 %) | I 1 tilstand |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sjældent (1–4%) | I 1 tilstand |
| ADAadenosine deaminase | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
AtlasFrom traits to your genome
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