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Merkmal
Full lips
Klinische Bezeichnung: Thick vermilion border
Increased width of the skin of vermilion border region of upper lip.
Zusammenfassung
- Auch genannt
- Increased volume of lip, Plump lips, Prominent lips, Thick lips, Increased volume of lip vermillion
- Körpersystem
- Abnormality of head or neck
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Diese Seite als Daten
Hängen Sie .json an die Adresse der Seite an oder fordern Sie application/json an, um sie als JSON zu lesen.
library(jsonlite)
url <- "https://dantelabs.com/traits/thick-vermilion-border.json"
page <- fromJSON(url)
page$trait$nameFull lipsHP:0012471
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AnmeldenFragenIhr Genom sequenzieren↗
Lesen Sie die Gene aus, die mit Full lips zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen75 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.
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- Intellectual DisabilityReads 30 of these genesARID1AATRXAUTS2FBXO11FBXO31KDM6BAbout this report →
- Ectodermal DysplasiasReads 6 of these genesEDATSPEAREDAREDARADDKDF1KREMEN1About this report →
- Cantú SyndromeReads 2 of these genesABCC9KCNJ8About this report →
Show 71 more reports
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 2 of these genesAIPGPR101About this report →
- Coffin-Siris SyndromeReads 4 of these genesARID1ASMARCB1SOX11SOX4About this report →
- Hypertrophic CardiomyopathyReads 9 of these genesERFMRASSOS1BRAFKRASMAP2K1About this report →
- Hypodontia and AnodontiaReads 3 of these genesEDATSPEARLRP6About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 5 of these genesRNU4-2TFE3TBCKZMYM2AP1S2About this report →
- Molybdenum Cofactor & Isolated Sulfite Oxidase DeficiencyReads 2 of these genesMOCS1MOCS2About this report →
- NeurofibromatosisReads 2 of these genesSMARCB1NF1About this report →
- Alzahrani-Kuwahara SyndromeReads 1 of these genesSMG8About this report →
- CWC27-Related Retinitis Pigmentosa with Skeletal AnomaliesReads 1 of these genesCWC27About this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Frank-Ter Haar SyndromeReads 1 of these genesSH3PXD2BAbout this report →
- GAPO SyndromeReads 1 of these genesANTXR1About this report →
- Jaberi-Elahi SyndromeReads 1 of these genesGTPBP2About this report →
- JARID2-Related Neurodevelopmental DisorderReads 1 of these genesJARID2About this report →
- KCNH1-Related DisorderReads 1 of these genesKCNH1About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- Meier-Gorlin Syndrome 4Reads 1 of these genesCDT1About this report →
- Meier-Gorlin Syndrome 7 (CDC45)Reads 1 of these genesCDC45About this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Mucopolysaccharidosis-Plus SyndromeReads 1 of these genesVPS33AAbout this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- PPP1R21-Related Neurodevelopmental DisorderReads 1 of these genesPPP1R21About this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Skraban-Deardorff SyndromeReads 1 of these genesWDR26About this report →
- Spondyloepimetaphyseal Dysplasia, Genevieve TypeReads 1 of these genesNANSAbout this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- Vici SyndromeReads 1 of these genesEPG5About this report →
- Congenital Disorders of GlycosylationReads 8 of these genesSRD5A3PIGLCOG6EDEM3MAN1B1COG7About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 2 of these genesAGANAGAAbout this report →
- DOORS SyndromeReads 1 of these genesATP6V1B2About this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Lysosomal Storage DiseaseReads 5 of these genesGNPTABIDUAAGAGNSNAGAAbout this report →
- Epilepsy (Full Panel)Reads 9 of these genesADAM22ATP6V1B2CDKL5DOCK7FLNAGRIA3About this report →
- Syndromic CraniosynostosisReads 3 of these genesERFIFT52RNU12About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesKIFBPAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Monogenic Precocious PubertyReads 1 of these genesDLK1About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 1 of these genesSMARCB1About this report →
- Inherited Congenital Heart DefectsReads 2 of these genesTFAP2BFLNAAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 2 of these genesKIF11SOX18About this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesSOX11About this report →
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 1 of these genesGNSAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Dilated CardiomyopathyReads 3 of these genesABCC9FHL1RAF1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesIFT52About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesXYLT1About this report →
- Joubert Syndrome And Related DisordersReads 2 of these genesOFD1KIF7About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Cutis LaxaReads 1 of these genesRIN2About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesCITAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGLAbout this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Ehlers-Danlos SyndromeReads 1 of these genesADAMTS2About this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesSNX14AIMP2TBCKAP4S1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesAIMP2About this report →
- Diabetes MellitusReads 1 of these genesEIF2S3About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSNX14About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesAP4S1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesAIMP2About this report →
- Retinitis PigmentosaReads 1 of these genesOFD1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesKRASAbout this report →
Lesen Sie die Gene aus, die mit Full lips zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen171 Gene mit Full lips verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Full lips auftritt. Die meisten Menschen mit diesem Merkmal haben keine dieser Erkrankungen, und ein Gen auf dieser Liste sagt nichts über das eigene Genom einer Person aus.
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| ADAM22ADAM metallopeptidase domain 22 | Immer | In 1 Erkrankung |
| ANTXR1ANTXR cell adhesion molecule 1 | Immer | In 1 Erkrankung |
| ARID1AAT-rich interaction domain 1A | Immer | In 1 Erkrankung |
| ATRXATRX chromatin remodeler | Immer | In 1 Erkrankung |
| AUTS2activator of transcription and developmental regulator AUTS2 | Immer | In 1 Erkrankung |
| BCAS3BCAS3 microtubule associated cell migration factor | Immer | In 1 Erkrankung |
| CCDC47coiled-coil domain containing 47 | Immer | In 1 Erkrankung |
| CDC6cell division cycle 6 | Immer | In 2 Erkrankungen |
| CITcitron rho-interacting serine/threonine kinase | Immer | In 1 Erkrankung |
| DONSONDNA replication fork stabilization factor DONSON | Immer | In 1 Erkrankung |
| EDAectodysplasin A | Immer | In 1 Erkrankung |
| ERFETS2 repressor factor | Immer | In 1 Erkrankung |
| EXOSC1exosome component 1 | Immer | In 1 Erkrankung |
| FBXO11F-box protein 11 | Immer | In 1 Erkrankung |
| FBXO31F-box protein 31 | Immer | In 1 Erkrankung |
| FIBPFGF1 intracellular binding protein | Immer | In 2 Erkrankungen |
| GMNNgeminin DNA replication inhibitor | Immer | In 2 Erkrankungen |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Immer | In 1 Erkrankung |
| GTPBP2GTP binding protein 2 | Immer | In 1 Erkrankung |
| IDUAalpha-L-iduronidase | Immer | In 4 Erkrankungen |
| IFT52intraflagellar transport 52 | Immer | In 1 Erkrankung |
| INSRinsulin receptor | Immer | In 2 Erkrankungen |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Immer | In 3 Erkrankungen |
| KDM6Blysine demethylase 6B | Immer | In 1 Erkrankung |
| MCM5minichromosome maintenance complex component 5 | Immer | In 1 Erkrankung |
| MED16mediator complex subunit 16 | Immer | In 1 Erkrankung |
| MRASmuscle RAS oncogene homolog | Immer | In 1 Erkrankung |
| NAV3neuron navigator 3 | Immer | In 1 Erkrankung |
| OFD1OFD1 centriole and centriolar satellite protein | Immer | In 1 Erkrankung |
| OGTO-linked N-acetylglucosamine (GlcNAc) transferase | Immer | In 1 Erkrankung |
| ORC6origin recognition complex subunit 6 | Immer | In 2 Erkrankungen |
| RBL2RB transcriptional corepressor like 2 | Immer | In 1 Erkrankung |
| RIN2Ras and Rab interactor 2 | Immer | In 1 Erkrankung |
| RNU4ATACRNA, U4atac small nuclear | Immer | In 2 Erkrankungen |
| SEC31ASEC31 homolog A, COPII component | Immer | In 1 Erkrankung |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Immer | In 1 Erkrankung |
| SNX14sorting nexin 14 | Immer | In 2 Erkrankungen |
| SRD5A3steroid 5 alpha-reductase 3 | Immer | In 1 Erkrankung |
| TAF4TATA-box binding protein associated factor 4 | Immer | In 1 Erkrankung |
| TSPEARthrombospondin type laminin G domain and EAR repeats | Immer | In 1 Erkrankung |
131 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| VPS13Bvacuolar protein sorting 13 homolog B | Immer | In 1 Erkrankung |
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Immer | In 1 Erkrankung |
| ABCC9ATP binding cassette subfamily C member 9 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| AGAaspartylglucosaminidase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| EIF2S3eukaryotic translation initiation factor 2 subunit gamma | Sehr häufig (80–99 %) | In 1 Erkrankung |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| RSPRY1ring finger and SPRY domain containing 1 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SH3PXD2BSH3 and PX domains 2B | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TCF4transcription factor 4 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TFAP2Btranscription factor AP-2 beta | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ACSL4acyl-CoA synthetase long chain family member 4 | Häufig (30–79 %) | In 1 Erkrankung |
| AFF2ALF transcription elongation factor 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| AIMP2aminoacyl tRNA synthetase complex interacting multifunctional protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| AIPAHR interacting HSP90 co-chaperone | Häufig (30–79 %) | In 1 Erkrankung |
| AMMECR1AMMECR nuclear protein 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Häufig (30–79 %) | In 1 Erkrankung |
| BORCS8BLOC-1 related complex subunit 8 | Häufig (30–79 %) | In 1 Erkrankung |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Häufig (30–79 %) | In 2 Erkrankungen |
| CBLCbl proto-oncogene | Häufig (30–79 %) | In 1 Erkrankung |
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Häufig (30–79 %) | In 1 Erkrankung |
| CDKL5cyclin dependent kinase like 5 | Häufig (30–79 %) | In 1 Erkrankung |
| CNTNAP1contactin associated protein 1 | Häufig (30–79 %) | In 1 Erkrankung |
| CNTNAP2contactin associated protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| COG6component of oligomeric golgi complex 6 | Häufig (30–79 %) | In 1 Erkrankung |
| DOCK7dedicator of cytokinesis 7 | Häufig (30–79 %) | In 2 Erkrankungen |
| ERMARDER membrane associated RNA degradation | Häufig (30–79 %) | In 1 Erkrankung |
| EXOSC5exosome component 5 | Häufig (30–79 %) | In 1 Erkrankung |
| FHL1four and a half LIM domains 1 | Häufig (30–79 %) | In 1 Erkrankung |
| FLNAfilamin A | Häufig (30–79 %) | In 2 Erkrankungen |
| FOXP1forkhead box P1 | Häufig (30–79 %) | In 1 Erkrankung |
| FRA10AC1FRA10A associated CGG repeat 1 | Häufig (30–79 %) | In 1 Erkrankung |
| GNSglucosamine (N-acetyl)-6-sulfatase | Häufig (30–79 %) | In 1 Erkrankung |
| GPC3glypican 3 | Häufig (30–79 %) | In 1 Erkrankung |
| GPR101G protein-coupled receptor 101 | Häufig (30–79 %) | In 1 Erkrankung |
| GTPBP1GTP binding protein 1 | Häufig (30–79 %) | In 1 Erkrankung |
| JARID2jumonji and AT-rich interaction domain containing 2 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNE5potassium voltage-gated channel subfamily E regulatory subunit 5 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNK9potassium two pore domain channel subfamily K member 9 | Häufig (30–79 %) | In 1 Erkrankung |
| KRASKRas proto-oncogene, GTPase | Häufig (30–79 %) | In 1 Erkrankung |
| LARP7La ribonucleoprotein 7, transcriptional regulator | Häufig (30–79 %) | In 2 Erkrankungen |
| LTBP3latent transforming growth factor beta binding protein 3 | Häufig (30–79 %) | In 1 Erkrankung |
| MAP2K1mitogen-activated protein kinase kinase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| MAP2K2mitogen-activated protein kinase kinase 2 | Häufig (30–79 %) | In 1 Erkrankung |
| MARK2microtubule affinity regulating kinase 2 | Häufig (30–79 %) | In 1 Erkrankung |
| MED12mediator complex subunit 12 | Häufig (30–79 %) | In 1 Erkrankung |
| NAGAalpha-N-acetylgalactosaminidase | Häufig (30–79 %) | In 1 Erkrankung |
| NF1neurofibromin 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| NFIXnuclear factor I X | Häufig (30–79 %) | In 1 Erkrankung |
| OBSL1obscurin like cytoskeletal adaptor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ORC1origin recognition complex subunit 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| PPP1R21protein phosphatase 1 regulatory subunit 21 | Häufig (30–79 %) | In 1 Erkrankung |
| PRIM1DNA primase subunit 1 | Häufig (30–79 %) | In 1 Erkrankung |
| PTDSS1phosphatidylserine synthase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| PUS7pseudouridine synthase 7 | Häufig (30–79 %) | In 1 Erkrankung |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Häufig (30–79 %) | In 1 Erkrankung |
| RNF2ring finger protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| RNU12RNA, U12 small nuclear | Häufig (30–79 %) | In 1 Erkrankung |
| RNU4-2RNA, U4 small nuclear 2 | Häufig (30–79 %) | In 1 Erkrankung |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Häufig (30–79 %) | In 1 Erkrankung |
| SOX11SRY-box transcription factor 11 | Häufig (30–79 %) | In 1 Erkrankung |
| SOX4SRY-box transcription factor 4 | Häufig (30–79 %) | In 1 Erkrankung |
| STAG2STAG2 cohesin complex component | Häufig (30–79 %) | In 1 Erkrankung |
| TFE3transcription factor binding to IGHM enhancer 3 | Häufig (30–79 %) | In 1 Erkrankung |
| TRIOtrio Rho guanine nucleotide exchange factor | Häufig (30–79 %) | In 1 Erkrankung |
| WDR26WD repeat domain 26 | Häufig (30–79 %) | In 1 Erkrankung |
| XYLT1xylosyltransferase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ADAT3adenosine deaminase tRNA specific 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| ANKRD11ankyrin repeat domain 11 | Manchmal (5–29 %) | In 1 Erkrankung |
| CACNA1Icalcium voltage-gated channel subunit alpha1 I | Manchmal (5–29 %) | In 1 Erkrankung |
| CDC45cell division cycle 45 | Manchmal (5–29 %) | In 1 Erkrankung |
| CDT1chromatin licensing and DNA replication factor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| DLK1delta like non-canonical Notch ligand 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| DOT1LDOT1 like histone lysine methyltransferase | Manchmal (5–29 %) | In 1 Erkrankung |
| DPYSL5dihydropyrimidinase like 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| EDARectodysplasin A receptor | Manchmal (5–29 %) | In 2 Erkrankungen |
| EDARADDEDAR associated via death domain | Manchmal (5–29 %) | In 2 Erkrankungen |
| EDEM3ER degradation enhancing alpha-mannosidase like protein 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| GRIA3glutamate ionotropic receptor AMPA type subunit 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| GTF3C3general transcription factor IIIC subunit 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| H4C5H4 clustered histone 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| HECTD4HECT domain E3 ubiquitin protein ligase 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| HNRNPH2heterogeneous nuclear ribonucleoprotein H2 | Manchmal (5–29 %) | In 1 Erkrankung |
| KAT8lysine acetyltransferase 8 | Manchmal (5–29 %) | In 1 Erkrankung |
| KDF1keratinocyte differentiation factor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| KDM2Blysine demethylase 2B | Manchmal (5–29 %) | In 1 Erkrankung |
| KIF11kinesin family member 11 | Manchmal (5–29 %) | In 1 Erkrankung |
| KIF15kinesin family member 15 | Manchmal (5–29 %) | In 1 Erkrankung |
| KIF7kinesin family member 7 | Manchmal (5–29 %) | In 1 Erkrankung |
| KREMEN1kringle containing transmembrane protein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| LRP6LDL receptor related protein 6 | Manchmal (5–29 %) | In 1 Erkrankung |
| MADDMAP kinase activating death domain | Manchmal (5–29 %) | In 1 Erkrankung |
| MEG3maternally expressed 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| NONOnon-POU domain containing octamer binding | Manchmal (5–29 %) | In 1 Erkrankung |
| ORC4origin recognition complex subunit 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| PCDHGC4protocadherin gamma subfamily C, 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| PIDD1p53-induced death domain protein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| PPP3CAprotein phosphatase 3 catalytic subunit alpha | Manchmal (5–29 %) | In 1 Erkrankung |
| RPL17ribosomal protein L17 | Manchmal (5–29 %) | In 1 Erkrankung |
| RTL1retrotransposon Gag like 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SETSET nuclear proto-oncogene | Manchmal (5–29 %) | In 1 Erkrankung |
| SETBP1SET binding protein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SMG8SMG8 nonsense mediated mRNA decay factor | Manchmal (5–29 %) | In 1 Erkrankung |
| SPENspen family transcriptional repressor | Manchmal (5–29 %) | In 1 Erkrankung |
| SPRED2sprouty related EVH1 domain containing 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| SUPT16HSPT16 homolog, facilitates chromatin remodeling subunit | Manchmal (5–29 %) | In 1 Erkrankung |
| TBCKTBC1 domain containing kinase | Manchmal (5–29 %) | In 1 Erkrankung |
| TRAF6TNF receptor associated factor 6 | Manchmal (5–29 %) | In 1 Erkrankung |
| USP9Xubiquitin specific peptidase 9 X-linked | Manchmal (5–29 %) | In 1 Erkrankung |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Manchmal (5–29 %) | In 2 Erkrankungen |
| WBP4WW domain binding protein 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| ZMYM2zinc finger MYM-type containing 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| ZNF699zinc finger protein 699 | Manchmal (5–29 %) | In 1 Erkrankung |
| EPG5ectopic P-granules 5 autophagy tethering factor | Selten (1–4 %) | In 1 Erkrankung |
| MAN1B1mannosidase alpha class 1B member 1 | Selten (1–4 %) | In 1 Erkrankung |
| SPTBN1spectrin beta, non-erythrocytic 1 | Selten (1–4 %) | In 1 Erkrankung |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Nicht erfasst | In 1 Erkrankung |
| AP1S2adaptor related protein complex 1 subunit sigma 2 | Nicht erfasst | In 1 Erkrankung |
| AP4S1adaptor related protein complex 4 subunit sigma 1 | Nicht erfasst | In 1 Erkrankung |
| COG7component of oligomeric golgi complex 7 | Nicht erfasst | In 1 Erkrankung |
| CWC27CWC27 spliceosome associated cyclophilin | Nicht erfasst | In 1 Erkrankung |
| GALNT2polypeptide N-acetylgalactosaminyltransferase 2 | Nicht erfasst | In 1 Erkrankung |
| KIFBPkinesin family binding protein | Nicht erfasst | In 1 Erkrankung |
| MOCS1molybdenum cofactor synthesis 1 | Nicht erfasst | In 1 Erkrankung |
| MOCS2molybdenum cofactor synthesis 2 | Nicht erfasst | In 1 Erkrankung |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Nicht erfasst | In 1 Erkrankung |
| NANSN-acetylneuraminate synthase | Nicht erfasst | In 1 Erkrankung |
| SLC35A2solute carrier family 35 member A2 | Nicht erfasst | In 1 Erkrankung |
| SOX18SRY-box transcription factor 18 | Nicht erfasst | In 1 Erkrankung |
Wie häufig dieses Merkmal bei Menschen mit einer der Erkrankungen auftritt, die mit dem Gen in Verbindung stehen, und zwar der höchste Wert unter ihnen, so wie ihn die Human Phenotype Ontology erfasst. Diese Seiten beschreiben Merkmale und die dazugehörige Forschung; sie stellen keine Diagnose dar. Fragen zu Symptomen richten Sie bitte an Ihre Ärztin, Ihren Arzt oder eine genetische Beratung.
Untergeordnete Merkmale
Übergeordnete Merkmale
Woher diese Angaben stammen
- Die Human Phenotype Ontology, Version 2026-09-01: das Merkmal, seine Bezeichnungen, seine Definition und die damit verknüpften Gene. Weitere Informationen finden Sie unter hpo.jax.org.
- Datenstand 2026.10.19-9814e911.
AtlasFür wen wir da sindUnsere WissenschaftProdukteErgebnisse
AnmeldenFragenIhr Genom sequenzieren↗
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.
Ab 449 $
Kostenloser Versand · Ergebnisse in 6–8 Wochen
