AtlasPožymis
Oligodactyly
A developmental defect resulting in the presence of fewer than the normal number of digits.
Santrauka
AtlasŠi puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/oligodactyly.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Oligodactyly, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test18 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.
- Cornelia de Lange SyndromeReads 6 of these genesBRD4HDAC8NIPBLRAD21SMC1ASMC3About this report →
- Cenani-Lenz Syndactyly SyndromeReads 1 of these genesLRP4About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
Show 14 more reports
- Rothmund-Thomson SyndromeReads 1 of these genesRECQL4About this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesRIPK4About this report →
- Syndromic CraniosynostosisReads 2 of these genesRECQL4CYP26B1About this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAPCAbout this report →
- Hypodontia and AnodontiaReads 1 of these genesWNT10BAbout this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- Inherited IchthyosesReads 1 of these genesNSDHLAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- Osteogenesis ImperfectaReads 1 of these genesMBTPS2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesMBTPS2About this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Intellectual DisabilityReads 2 of these genesBRD4NSDHLAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesSMC1AAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Oligodactyly, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test28 genų susiję su Oligodactyly
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Oligodactyly. 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 |
|---|---|---|
| FAAP100FA core complex associated protein 100 | Visada | 1 ligoje |
| RIPK4receptor interacting serine/threonine kinase 4 | Visada | 1 ligoje |
| APCAPC regulator of Wnt signaling pathway | Labai dažnai (80–99%) | 1 ligoje |
| BTRCbeta-transducin repeat containing E3 ubiquitin protein ligase | Labai dažnai (80–99%) | 1 ligoje |
| DLX5distal-less homeobox 5 | Labai dažnai (80–99%) | 1 ligoje |
| DLX6distal-less homeobox 6 | Labai dažnai (80–99%) | 1 ligoje |
| EPS15L1epidermal growth factor receptor pathway substrate 15 like 1 | Labai dažnai (80–99%) | 1 ligoje |
| FBXW4F-box and WD repeat domain containing 4 | Labai dažnai (80–99%) | 1 ligoje |
| LRP4LDL receptor related protein 4 | Labai dažnai (80–99%) | 1 ligoje |
| SEM1SEM1 26S proteasome subunit | Labai dažnai (80–99%) | 1 ligoje |
| TP63tumor protein p63 | Labai dažnai (80–99%) | 3 ligose |
| WNT10BWnt family member 10B | Labai dažnai (80–99%) | 1 ligoje |
| H4C3H4 clustered histone 3 | Dažnai (30–79%) | 1 ligoje |
| RECQL4RecQ like helicase 4 | Dažnai (30–79%) | 1 ligoje |
| BRD4bromodomain containing 4 | Kartais (5–29%) | 1 ligoje |
| GLI3GLI family zinc finger 3 | Kartais (5–29%) | 3 ligose |
| HDAC8histone deacetylase 8 | Kartais (5–29%) | 1 ligoje |
| MAU2MAU2 sister chromatid cohesion factor | Kartais (5–29%) | 1 ligoje |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Kartais (5–29%) | 1 ligoje |
| NIPBLNIPBL cohesin loading factor | Kartais (5–29%) | 2 ligose |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Kartais (5–29%) | 1 ligoje |
| RAD21RAD21 cohesin complex component | Kartais (5–29%) | 1 ligoje |
| SMC1Astructural maintenance of chromosomes 1A | Kartais (5–29%) | 1 ligoje |
| SMC3structural maintenance of chromosomes 3 | Kartais (5–29%) | 1 ligoje |
| CYP26B1cytochrome P450 family 26 subfamily B member 1 | Neužfiksuota | 1 ligoje |
| DONSONDNA replication fork stabilization factor DONSON | Neužfiksuota | 1 ligoje |
| HOXD13homeobox D13 | Neužfiksuota | 1 ligoje |
| WNT7AWnt family member 7A | 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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Iš kur tai žinoma
- 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.
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