AtlasÖzellik
Abnormal circulating lipid concentration
Any deviation from the normal concentration of lipid in the blood circulation.
Özet
- Diğer adları
- Abnormal lipid level
- Vücut sistemi
- Laboratory abnormality
AtlasBu sayfanın veri olarak görünümü
Veriyi JSON olarak okumak için sayfa adresinin sonuna .json ekleyin veya application/json isteyin.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-circulating-lipid-concentration.json"
page <- fromJSON(url)
page$trait$nameAbnormal circulating lipid concentration ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi al27 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.
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
Show 23 more reports
- Hereditary HypolipoproteinemiasReads 2 of these genesABCA1APOA1About this report →
- CitrullinemiaReads 1 of these genesSLC25A13About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12RB1About this report →
- HyperinsulinismReads 1 of these genesABCC8About this report →
- Hereditary AmyloidosisReads 1 of these genesAPOA1About this report →
- LipodystrophyReads 1 of these genesLIPEAbout this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesABCC8About this report →
- Urea Cycle DisorderReads 1 of these genesSLC25A13About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesGLASMPD1About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 1 of these genesHRAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesARAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesABCC8About this report →
- Diabetes MellitusReads 1 of these genesABCC8About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTNPO3About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
- Epilepsy (Full Panel)Reads 1 of these genesLMNB2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNCF1About this report →
Abnormal circulating lipid concentration ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alAbnormal circulating lipid concentration ile ilişkili 40 gen
Bu genlerdeki değişiklikler, Abnormal circulating lipid concentration 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 |
|---|---|---|
| ABCC8ATP binding cassette subfamily C member 8 | Her zaman | 1 durumda |
| LAMB1laminin subunit beta 1 | Her zaman | 1 durumda |
| ABCA1ATP binding cassette subfamily A member 1 | Çok sık (%80–99) | 1 durumda |
| APOA1apolipoprotein A1 | Çok sık (%80–99) | 1 durumda |
| SLC25A13solute carrier family 25 member 13 | Çok sık (%80–99) | 1 durumda |
| GLAgalactosidase alpha | Sık (%30–79) | 1 durumda |
| IL12Ainterleukin 12A | Sık (%30–79) | 1 durumda |
| IL12RB1interleukin 12 receptor subunit beta 1 | Sık (%30–79) | 1 durumda |
| IRF5interferon regulatory factor 5 | Sık (%30–79) | 1 durumda |
| MMEL1membrane metalloendopeptidase like 1 | Sık (%30–79) | 1 durumda |
| POU2AF1POU class 2 homeobox associating factor 1 | Sık (%30–79) | 1 durumda |
| SMPD1sphingomyelin phosphodiesterase 1 | Sık (%30–79) | 1 durumda |
| SPIBSpi-B transcription factor | Sık (%30–79) | 1 durumda |
| TBCKTBC1 domain containing kinase | Sık (%30–79) | 1 durumda |
| TNFSF15TNF superfamily member 15 | Sık (%30–79) | 1 durumda |
| TNPO3transportin 3 | Sık (%30–79) | 1 durumda |
| ARandrogen receptor | Bazen (%5–29) | 1 durumda |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Bazen (%5–29) | 1 durumda |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Bazen (%5–29) | 1 durumda |
| CLIP2CAP-Gly domain containing linker protein 2 | Bazen (%5–29) | 1 durumda |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Bazen (%5–29) | 1 durumda |
| EIF4Heukaryotic translation initiation factor 4H | Bazen (%5–29) | 1 durumda |
| ELNelastin | Bazen (%5–29) | 1 durumda |
| FBN1fibrillin 1 | Bazen (%5–29) | 1 durumda |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Bazen (%5–29) | 1 durumda |
| GTF2Igeneral transcription factor IIi | Bazen (%5–29) | 1 durumda |
| GTF2IRD1GTF2I repeat domain containing 1 | Bazen (%5–29) | 1 durumda |
| GTF2IRD2GTF2I repeat domain containing 2 | Bazen (%5–29) | 1 durumda |
| HRHR lysine demethylase and nuclear receptor corepressor | Bazen (%5–29) | 1 durumda |
| LIMK1LIM domain kinase 1 | Bazen (%5–29) | 1 durumda |
| METTL27methyltransferase like 27 | Bazen (%5–29) | 1 durumda |
| NCF1neutrophil cytosolic factor 1 | Bazen (%5–29) | 1 durumda |
| RFC2replication factor C subunit 2 | Bazen (%5–29) | 1 durumda |
| STX1Asyntaxin 1A | Bazen (%5–29) | 1 durumda |
| TBL2transducin beta like 2 | Bazen (%5–29) | 1 durumda |
| TMEM270transmembrane protein 270 | Bazen (%5–29) | 1 durumda |
| VPS37DVPS37D subunit of ESCRT-I | Bazen (%5–29) | 1 durumda |
| LIPElipase E, hormone sensitive type | Kaydedilmedi | 1 durumda |
| LMNB2lamin B2 | Kaydedilmedi | 1 durumda |
| XRCC4X-ray repair cross complementing 4 | 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 dar özellikler
- Elevated lipids in blood45 gen
- Abnormality of cholesterol metabolism6 gen
- Abnormal circulating fatty acid concentration2 gen
- Elevated circulating C-triol concentration2 gen
- Elevated circulating sitosterol concentration2 gen
- Elevated circulating dimethyl sterol concentration1 gen
- Elevated circulating lysosphingomyelin concentration1 gen
- Elevated circulating methysterol concentration1 gen
- Elevated circulating monomethyl sterol concentration1 gen
- Hyperapobetalipoproteinemia1 gen
- Increased circulating farnesol concentration1 gen
- Abnormal circulating beta-carotene concentration
- Abnormal circulating phospholipid concentration
- Hypolipidemia
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 2026.10.16-c6eea6bf.
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