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Özellik
Enlarged kidney
An abnormal increase in the size of the kidney.
Özet
- Diğer adları
- Large kidneys, Nephromegaly, Renal enlargement
- Vücut sistemi
- Abnormality of the genitourinary system
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Veriyi JSON olarak okumak için sayfa adresinin sonuna .json ekleyin veya application/json isteyin.
library(jsonlite)
url <- "https://dantelabs.com/traits/enlarged-kidney.json"
page <- fromJSON(url)
page$trait$nameEnlarged kidneyHP:0000105
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Enlarged kidney ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
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Genome Test'imi al40 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.
- Polycystic Kidney DiseaseReads 10 of these genesDZIP1LPKHD1NEK8ALG5ALG9DNAJB11About this report →
- Cardiac-Urogenital SyndromeReads 1 of these genesMYRFAbout this report →
- DICER1 Tumour PredispositionReads 1 of these genesDICER1About this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
Show 36 more reports
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- Jeune Asphyxiating Thoracic Dystrophy (DYNC2H1)Reads 1 of these genesDYNC2H1About this report →
- Mucopolysaccharidosis-Plus SyndromeReads 1 of these genesVPS33AAbout this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 4 of these genesANKS6NEK8NPHP3INVSAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Lung CancerReads 1 of these genesDICER1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesCDKN1CIGF2About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- TyrosinemiaReads 1 of these genesFAHAbout this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC37A4G6PC1About this report →
- Familial Atrial FibrillationReads 1 of these genesKCNQ1About this report →
- Short Qt SyndromeReads 1 of these genesKCNQ1About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- PancreatitisReads 1 of these genesTRPV6About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesPRKAG2About this report →
- Hypertrophic CardiomyopathyReads 3 of these genesPRKAG2CDKN1CIGF2About this report →
- Long QT SyndromeReads 1 of these genesKCNQ1About this report →
- Meckel SyndromeReads 1 of these genesTCTN2About this report →
- Familial HypomagnesemiaReads 1 of these genesTRPV6About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesZIC3About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Severe Congenital NeutropeniaReads 1 of these genesVPS45About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesWT1About this report →
- Retinitis PigmentosaReads 2 of these genesFLVCR1IFT140About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesSLC37A4ALG9About this report →
- Thyroid CancerReads 1 of these genesTRPV6About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesTCTN2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesFLVCR1About this report →
- Intellectual DisabilityReads 2 of these genesADNPNAA10About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGNPTABAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesFLVCR1About this report →
Enlarged kidney ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alEnlarged kidney ile ilişkili 48 gen
Bu genlerdeki değişiklikler, Enlarged kidney özelliğinin görüldüğü nadir durumlara yol açar. Bu özelliğe sahip çoğu kişide bu durumlardan hiçbiri yoktur; ayrıca bu listedeki bir gen, kimsenin kendi genomu hakkında bir şey söylemez.
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| CD81CD81 molecule | Her zaman | 1 durumda |
| CPT2carnitine palmitoyltransferase 2 | Her zaman | 1 durumda |
| FLVCR1FLVCR choline and heme transporter 1 | Her zaman | 1 durumda |
| VPS45vacuolar protein sorting 45 homolog | Her zaman | 1 durumda |
| WT1WT1 transcription factor | Her zaman | 2 durumda |
| DZIP1LDAZ interacting zinc finger protein 1 like | Çok sık (%80–99) | 2 durumda |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Çok sık (%80–99) | 2 durumda |
| ANKS6ankyrin repeat and sterile alpha motif domain containing 6 | Sık (%30–79) | 1 durumda |
| DICER1dicer 1, ribonuclease III | Sık (%30–79) | 1 durumda |
| FAHfumarylacetoacetate hydrolase | Sık (%30–79) | 1 durumda |
| INSRinsulin receptor | Sık (%30–79) | 2 durumda |
| MYRFmyelin regulatory factor | Sık (%30–79) | 1 durumda |
| NEK8NIMA related kinase 8 | Sık (%30–79) | 4 durumda |
| NPHP3nephrocystin 3 | Sık (%30–79) | 3 durumda |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Sık (%30–79) | 1 durumda |
| RBSNrabenosyn, RAB effector | Sık (%30–79) | 1 durumda |
| SAA1serum amyloid A1 | Sık (%30–79) | 1 durumda |
| SLC37A4solute carrier family 37 member 4 | Sık (%30–79) | 2 durumda |
| ZIC3Zic family zinc finger 3 | Sık (%30–79) | 2 durumda |
| ADNPactivity dependent neuroprotector homeobox | Bazen (%5–29) | 1 durumda |
| AKT1AKT serine/threonine kinase 1 | Bazen (%5–29) | 1 durumda |
| ALG5ALG5 dolichyl-phosphate beta-glucosyltransferase | Bazen (%5–29) | 1 durumda |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Bazen (%5–29) | 2 durumda |
| BICC1BicC family RNA binding protein 1 | Bazen (%5–29) | 1 durumda |
| DNAJB11DnaJ heat shock protein family (Hsp40) member B11 | Bazen (%5–29) | 1 durumda |
| FIBPFGF1 intracellular binding protein | Bazen (%5–29) | 1 durumda |
| GANABglucosidase II alpha subunit | Bazen (%5–29) | 1 durumda |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Bazen (%5–29) | 1 durumda |
| IFT140intraflagellar transport 140 | Bazen (%5–29) | 1 durumda |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Bazen (%5–29) | 1 durumda |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Bazen (%5–29) | 1 durumda |
| PKD1polycystin 1, transient receptor potential channel interacting | Bazen (%5–29) | 1 durumda |
| PKD2polycystin 2, transient receptor potential cation channel | Bazen (%5–29) | 1 durumda |
| SLC29A3solute carrier family 29 member 3 | Bazen (%5–29) | 1 durumda |
| TCTN2tectonic family member 2 | Bazen (%5–29) | 1 durumda |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Bazen (%5–29) | 1 durumda |
| TULP3TUB like protein 3 | Bazen (%5–29) | 1 durumda |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Bazen (%5–29) | 2 durumda |
| BMPERBMP binding endothelial regulator | Kaydedilmedi | 1 durumda |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Kaydedilmedi | 1 durumda |
8 gen daha göster
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| CILK1ciliogenesis associated kinase 1 | Kaydedilmedi | 1 durumda |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Kaydedilmedi | 1 durumda |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Kaydedilmedi | 1 durumda |
| GPC3glypican 3 | Kaydedilmedi | 1 durumda |
| IGF2insulin like growth factor 2 | Kaydedilmedi | 1 durumda |
| INVSinversin | Kaydedilmedi | 1 durumda |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Kaydedilmedi | 1 durumda |
| KCNQ1OT1KCNQ1 opposite strand/antisense transcript 1 | Kaydedilmedi | 1 durumda |
Bu özelliğin, genin ilişkili olduğu durumlardan birine sahip kişiler arasında ne sıklıkta görüldüğü; Human Phenotype Ontology'nin kaydettiği şekliyle, bunlar arasında en sık görülen oran. Bu sayfalar özellikleri ve bunların arkasındaki araştırmaları anlatır; tanı koymaz. Belirtiler hakkında bir doktora veya genetik danışmana başvurmanız gerekir.
Daha geniş özellikler
Bilgilerin kaynağı
- Human Phenotype Ontology, 2026-09-01 sürümü: özellik, adları, tanımı ve buna bağlı genler. Ayrıntılar için hpo.jax.org adresine bakın.
- Veri sürümü 2026.10.19-9814e911.
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
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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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