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PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Scaling skin
Refers to the loss of the outer layer of the epidermis in large, scale-like flakes.
Santrauka
- Taip pat vadinama
- flaking skin, peeling skin, Scaly skin, Desquamation
- Kūno sistema
- Abnormality of the integument
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/scaling-skin.json"
page <- fromJSON(url)
page$trait$nameScaling skinHP:0040189
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Scaling skin, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test42 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.
- Inherited IchthyosesReads 11 of these genesCDSNFLG2KRT1KRT10SERPINB8SULT2B1About this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- MEND SyndromeReads 1 of these genesEBPAbout this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
Show 38 more reports
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 5 of these genesKRT1GJB2GJB6GJA1MBTPS2About this report →
- Severe Combined ImmunodeficiencyReads 4 of these genesDCLRE1CRAG1RAG2CARMIL2About this report →
- LipodystrophyReads 2 of these genesZMPSTE24LMNAAbout this report →
- Stargardt DiseaseReads 1 of these genesELOVL4About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 2 of these genesCDSNKRT74About this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesKITAbout this report →
- Hereditary Vascular MalformationsReads 1 of these genesRASA1About this report →
- Moyamoya DiseaseReads 1 of these genesSAMHD1About this report →
- Other Inborn Errors of ImmunityReads 7 of these genesDCLRE1CIL2RARAG1RAG2SPINK5CARMIL2About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesADAM17About this report →
- Hyper-IgE SyndromeReads 1 of these genesSPINK5About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesIL2RAAbout this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesSAMHD1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesDCAF17About this report →
- Hereditary AmyloidosisReads 1 of these genesOSMRAbout this report →
- Glycogen Storage DiseaseReads 1 of these genesLDHAAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesKIF11About this report →
- Ectodermal DysplasiasReads 1 of these genesGJB6About this report →
- Epidermolysis BullosaReads 1 of these genesPKP1About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesMPV17LMNAAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesIL2RAAbout this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesELOVL4DCAF17RNF168SAMHD1About this report →
- Hearing Loss and DeafnessReads 2 of these genesGJB2GJB6About this report →
- Diabetes MellitusReads 1 of these genesIL2RAAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesMBTPS2About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesSAMHD1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesELOVL4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesDCAF17About this report →
- DNA Repair DiseaseReads 1 of these genesDCLRE1CAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesDCAF17About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesRNF168About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesMPV17LMNAAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesSAMHD1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesMPDU1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesMPV17About this report →
Vienu tyrimu sužinokite genus, susijusius su Scaling skin, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test45 genų susiję su Scaling skin
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Scaling skin. 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 |
|---|---|---|
| CASTcalpastatin | Visada | 1 ligoje |
| CDSNcorneodesmosin | Visada | 2 ligose |
| DCLRE1CDNA cross-link repair 1C | Visada | 1 ligoje |
| DONSONDNA replication fork stabilization factor DONSON | Visada | 1 ligoje |
| ELOVL4ELOVL fatty acid elongase 4 | Visada | 1 ligoje |
| FLG2filaggrin 2 | Visada | 1 ligoje |
| IL2RAinterleukin 2 receptor subunit alpha | Visada | 1 ligoje |
| KRT1keratin 1 | Visada | 3 ligose |
| KRT10keratin 10 | Visada | 2 ligose |
| MPV17mitochondrial inner membrane protein MPV17 | Visada | 1 ligoje |
| PKP1plakophilin 1 | Visada | 2 ligose |
| PPP2R3Cprotein phosphatase 2 regulatory subunit B''gamma | Visada | 1 ligoje |
| RAG1recombination activating 1 | Visada | 1 ligoje |
| RAG2recombination activating 2 | Visada | 1 ligoje |
| SERPINB8serpin family B member 8 | Visada | 1 ligoje |
| SPINK5serine peptidase inhibitor Kazal type 5 | Visada | 1 ligoje |
| SULT2B1sulfotransferase family 2B member 1 | Visada | 1 ligoje |
| TGM5transglutaminase 5 | Visada | 2 ligose |
| ZMPSTE24zinc metallopeptidase STE24 | Visada | 2 ligose |
| LMNAlamin A/C | Labai dažnai (80–99%) | 1 ligoje |
| TGM1transglutaminase 1 | Labai dažnai (80–99%) | 1 ligoje |
| ADAM17ADAM metallopeptidase domain 17 | Dažnai (30–79%) | 1 ligoje |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Dažnai (30–79%) | 1 ligoje |
| CSTAcystatin A | Dažnai (30–79%) | 2 ligose |
| EBPEBP cholestenol delta-isomerase | Dažnai (30–79%) | 1 ligoje |
| GJB2gap junction protein beta 2 | Dažnai (30–79%) | 1 ligoje |
| GJB6gap junction protein beta 6 | Dažnai (30–79%) | 1 ligoje |
| LDHAlactate dehydrogenase A | Dažnai (30–79%) | 1 ligoje |
| RECQLRecQ like helicase | Dažnai (30–79%) | 1 ligoje |
| SASH1SAM and SH3 domain containing 1 | Dažnai (30–79%) | 1 ligoje |
| DCAF17DDB1 and CUL4 associated factor 17 | Kartais (5–29%) | 1 ligoje |
| GJA1gap junction protein alpha 1 | Kartais (5–29%) | 1 ligoje |
| GNB2G protein subunit beta 2 | Kartais (5–29%) | 1 ligoje |
| KIF11kinesin family member 11 | Kartais (5–29%) | 1 ligoje |
| KITKIT proto-oncogene, receptor tyrosine kinase | Kartais (5–29%) | 1 ligoje |
| KRT74keratin 74 | Kartais (5–29%) | 1 ligoje |
| MPDU1mannose-P-dolichol utilization defect 1 | Kartais (5–29%) | 2 ligose |
| RASA1RAS p21 protein activator 1 | Kartais (5–29%) | 1 ligoje |
| RNF168ring finger protein 168 | Kartais (5–29%) | 1 ligoje |
| CARD14caspase recruitment domain family member 14 | Neužfiksuota | 1 ligoje |
Rodyti dar 5 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| KLK11kallikrein related peptidase 11 | Neužfiksuota | 1 ligoje |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Neužfiksuota | 1 ligoje |
| NIPAL4NIPA like domain containing 4 | Neužfiksuota | 1 ligoje |
| OSMRoncostatin M receptor | Neužfiksuota | 1 ligoje |
| SAMHD1SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 | 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.
Siauresni požymiai
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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.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
From traits to your genome
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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