Tunnus
Wide nose
Interalar distance more than two standard deviations above the mean for age, i.e., an apparently increased width of the nasal base and alae.
Kokkuvõte
- Teised nimetused
- Broad nose, Increased breadth of nose, Increased nasal breadth, Increased nasal width, Increased width of nose
- Kehasüsteem
- Abnormality of head or neck
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/wide-nose.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud Wide nose-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test137 geeni on seotud tunnusega Wide nose
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Wide nose. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ARID2AT-rich interaction domain 2 | Alati | Esineb 1 haiguses |
| CCNQcyclin Q | Alati | Esineb 1 haiguses |
| CDH11cadherin 11 | Alati | Esineb 1 haiguses |
| CHD8chromodomain helicase DNA binding protein 8 | Alati | Esineb 1 haiguses |
| GPC4glypican 4 | Alati | Esineb 1 haiguses |
| GRIP1glutamate receptor interacting protein 1 | Alati | Esineb 1 haiguses |
| INTS11integrator complex subunit 11 | Alati | Esineb 1 haiguses |
| KDM2Blysine demethylase 2B | Alati | Esineb 1 haiguses |
| KDM6Alysine demethylase 6A | Alati | Esineb 1 haiguses |
| KDM6Blysine demethylase 6B | Alati | Esineb 1 haiguses |
| KMT2Dlysine methyltransferase 2D | Alati | Esineb 1 haiguses |
| LARP7La ribonucleoprotein 7, transcriptional regulator | Alati | Esineb 2 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| MOGSmannosyl-oligosaccharide glucosidase | Alati | Esineb 2 haiguses |
| PPFIA3PPFI scaffold protein A3 | Alati | Esineb 1 haiguses |
| PRRX1paired related homeobox 1 | Alati | Esineb 1 haiguses |
| SLC37A4solute carrier family 37 member 4 | Alati | Esineb 1 haiguses |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Alati | Esineb 1 haiguses |
| STAT3signal transducer and activator of transcription 3 | Alati | Esineb 1 haiguses |
| TAF4TATA-box binding protein associated factor 4 | Alati | Esineb 1 haiguses |
| UBR5ubiquitin protein ligase E3 component n-recognin 5 | Alati | Esineb 1 haiguses |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Alati | Esineb 1 haiguses |
| VPS53VPS53 subunit of GARP complex | Alati | Esineb 1 haiguses |
| WLSWnt ligand secretion mediator | Alati | Esineb 1 haiguses |
| ACTBactin beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| ACTG1actin gamma 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Väga sageli (80–99%) | Esineb 1 haiguses |
| CKAP2Lcytoskeleton associated protein 2L | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLCF1cardiotrophin like cytokine factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CRLF1cytokine receptor like factor 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| DVL1dishevelled segment polarity protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DVL3dishevelled segment polarity protein 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FZD2frizzled class receptor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GPR101G protein-coupled receptor 101 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KAT6Blysine acetyltransferase 6B | Väga sageli (80–99%) | Esineb 2 haiguses |
| MGPmatrix Gla protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SEC23ASEC23 homolog A, COPII component | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCTN3tectonic family member 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
Näita veel 97 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| TMCO1transmembrane and coiled-coil domains 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TRIM37tripartite motif containing 37 | Väga sageli (80–99%) | Esineb 1 haiguses |
| WNT5AWnt family member 5A | Väga sageli (80–99%) | Esineb 1 haiguses |
| YWHAEtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon | Väga sageli (80–99%) | Esineb 1 haiguses |
| ACBD6acyl-CoA binding domain containing 6 | Sageli (30–79%) | Esineb 1 haiguses |
| ARID1AAT-rich interaction domain 1A | Sageli (30–79%) | Esineb 1 haiguses |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Sageli (30–79%) | Esineb 1 haiguses |
| CAMTA1calmodulin binding transcription activator 1 | Sageli (30–79%) | Esineb 1 haiguses |
| COX7Bcytochrome c oxidase subunit 7B | Sageli (30–79%) | Esineb 1 haiguses |
| DPF2double PHD fingers 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DYNC2I1dynein 2 intermediate chain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DYNC2I2dynein 2 intermediate chain 2 | Sageli (30–79%) | Esineb 1 haiguses |
| FHL1four and a half LIM domains 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GON4Lgon-4 like | Sageli (30–79%) | Esineb 1 haiguses |
| HCCSholocytochrome c synthase | Sageli (30–79%) | Esineb 1 haiguses |
| IFT80intraflagellar transport 80 | Sageli (30–79%) | Esineb 1 haiguses |
| IL11RAinterleukin 11 receptor subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| KATNB1katanin regulatory subunit B1 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Sageli (30–79%) | Esineb 3 haiguses |
| KCNN3potassium calcium-activated channel subfamily N member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| KICS2KICSTOR subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MEGF8multiple EGF like domains 8 | Sageli (30–79%) | Esineb 1 haiguses |
| NDE1nudE neurodevelopment protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Sageli (30–79%) | Esineb 1 haiguses |
| NOTCH2notch receptor 2 | Sageli (30–79%) | Esineb 2 haiguses |
| OTUD6BOTU deubiquitinase 6B | Sageli (30–79%) | Esineb 1 haiguses |
| PHGDHphosphoglycerate dehydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Sageli (30–79%) | Esineb 1 haiguses |
| POU4F1POU class 4 homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| QRICH1glutamine rich 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RAB23RAB23, member RAS oncogene family | Sageli (30–79%) | Esineb 1 haiguses |
| RELNreelin | Sageli (30–79%) | Esineb 1 haiguses |
| RNF2ring finger protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RPS6KA3ribosomal protein S6 kinase A3 | Sageli (30–79%) | Esineb 3 haiguses |
| SETD1ASET domain containing 1A, histone lysine methyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| TRMT10AtRNA methyltransferase 10A | Sageli (30–79%) | Esineb 2 haiguses |
| TWIST2twist family bHLH transcription factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| WDR35WD repeat domain 35 | Sageli (30–79%) | Esineb 1 haiguses |
| ADAMTS18ADAM metallopeptidase with thrombospondin type 1 motif 18 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Mõnikord (5–29%) | Esineb 2 haiguses |
| ASPHaspartate beta-hydroxylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRCC3BRCA1/BRCA2-containing complex subunit 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BUB1BUB1 mitotic checkpoint serine/threonine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Mõnikord (5–29%) | Esineb 2 haiguses |
| BUB3BUB3 mitotic checkpoint protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| CEP57centrosomal protein 57 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COG8component of oligomeric golgi complex 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRELD1CRELD disulfide isomerase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DLK1delta like non-canonical Notch ligand 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| FREM2FRAS1 related extracellular matrix 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HMGA2high mobility group AT-hook 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| INSRinsulin receptor | Mõnikord (5–29%) | Esineb 2 haiguses |
| KIF11kinesin family member 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LEMD3LEM domain containing 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMBRD2LMBR1 domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMX1BLIM homeobox transcription factor 1 beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAN1B1mannosidase alpha class 1B member 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MEG3maternally expressed 3 | Mõnikord (5–29%) | Esineb 3 haiguses |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTENphosphatase and tensin homolog | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAI1retinoic acid induced 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNF125ring finger protein 125 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RTL1retrotransposon Gag like 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| SATB2SATB homeobox 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SETBP1SET binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMG9SMG9 nonsense mediated mRNA decay factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| STXBP1syntaxin binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBX1T-box transcription factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TOGARAM1TOG array regulator of axonemal microtubules 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TONSLtonsoku like, DNA repair protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIP13thyroid hormone receptor interactor 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| WBP11WW domain binding protein 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACY1aminoacylase 1 | Harva (1–4%) | Esineb 1 haiguses |
| EPG5ectopic P-granules 5 autophagy tethering factor | Harva (1–4%) | Esineb 1 haiguses |
| AVParginine vasopressin | Pole registreeritud | Esineb 1 haiguses |
| COG7component of oligomeric golgi complex 7 | Pole registreeritud | Esineb 1 haiguses |
| DONSONDNA replication fork stabilization factor DONSON | Pole registreeritud | Esineb 1 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Pole registreeritud | Esineb 1 haiguses |
| FRAS1Fraser extracellular matrix complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| FUCA1alpha-L-fucosidase 1 | Pole registreeritud | Esineb 1 haiguses |
| GDF5growth differentiation factor 5 | Pole registreeritud | Esineb 1 haiguses |
| HDAC4histone deacetylase 4 | Pole registreeritud | Esineb 1 haiguses |
| IDUAalpha-L-iduronidase | Pole registreeritud | Esineb 1 haiguses |
| KMT2Alysine methyltransferase 2A | Pole registreeritud | Esineb 1 haiguses |
| NANSN-acetylneuraminate synthase | Pole registreeritud | Esineb 1 haiguses |
| PAM16presequence translocase associated motor 16 | Pole registreeritud | Esineb 1 haiguses |
| SIN3ASIN3 transcription regulator family member A | Pole registreeritud | Esineb 1 haiguses |
| SKIC3SKI3 subunit of superkiller complex | Pole registreeritud | Esineb 1 haiguses |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Pole registreeritud | Esineb 1 haiguses |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Pole registreeritud | Esineb 1 haiguses |
| STAMBPSTAM binding protein | Pole registreeritud | Esineb 1 haiguses |
| TBL1XR1TBL1X/Y related 1 | Pole registreeritud | Esineb 1 haiguses |
| ZNF341zinc finger protein 341 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.17-8666dff2.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast