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Piirre
Postaxial polydactyly
A form of polydactyly in which the extra digit or digits are localized on the side of the fifth finger or fifth toe.
Yhteenveto
- Tunnetaan myös nimellä
- Polydactyly, postaxial, Postaxial hexadactyly
- Elimistön järjestelmä
- Abnormality of limbsAbnormality of the musculoskeletal system
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Tämä sivu datana
Lisää sivun osoitteen perään .json tai pyydä application/json-muotoa, niin saat sivun JSON-muodossa.
library(jsonlite)
url <- "https://dantelabs.com/traits/postaxial-polydactyly.json"
page <- fromJSON(url)
page$trait$namePostaxial polydactylyHP:0100259
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Lue Postaxial polydactyly-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test46 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.
- Bardet-Biedl and Alström SyndromesReads 22 of these genesARL6BBS7BBS9IFT74MKKSMKS1About this report →
- Joubert Syndrome And Related DisordersReads 14 of these genesB9D2MKS1TCTN3CEP290NPHP1TMEM231About this report →
- Meckel SyndromeReads 5 of these genesB9D2MKS1TMEM231TXNDC15RPGRIP1LAbout this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 3 of these genesIFT52IFT43WDR35About this report →
Show 42 more reports
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- INTU-Related Skeletal CiliopathyReads 1 of these genesINTUAbout this report →
- Jeune Asphyxiating Thoracic Dystrophy (DYNC2H1)Reads 1 of these genesDYNC2H1About this report →
- MEND SyndromeReads 1 of these genesEBPAbout this report →
- Short-Rib Thoracic Dysplasia 11 (DYNC2I2)Reads 1 of these genesDYNC2I2About this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- Short-Rib Thoracic Dysplasia 8 (DYNC2I1)Reads 1 of these genesDYNC2I1About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- TARP SyndromeReads 1 of these genesRBM10About this report →
- Syndromic CraniosynostosisReads 4 of these genesIFT52IFT43MEGF8WDR35About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 6 of these genesMKS1CEP290TMEM231CSPP1KIAA0586TMEM237About this report →
- Retinitis PigmentosaReads 7 of these genesARL6TTC8BBS2CFAP418IFT172IFT43About this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Inherited Congenital Heart DefectsReads 2 of these genesGATA6NKX2-5About this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesGDF6About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 2 of these genesNPHP1SDCCAG8About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3R2About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesSETD5ZFXAbout this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR2About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesCEP19About this report →
- GlomerulosclerosisReads 1 of these genesCRB2About this report →
- Intellectual DisabilityReads 5 of these genesSCAPERUSP9XSETD5SYNGAP1ZFXAbout this report →
- Focal Segmental GlomerulosclerosisReads 1 of these genesCRB2About this report →
- Marfan Like SyndromesReads 1 of these genesTGFBR2About this report →
- Inherited Neurodegenerative DisordersReads 6 of these genesMKS1CEP290TMEM231CSPP1KIAA0586TMEM237About this report →
- Aortic AneurysmReads 1 of these genesTGFBR2About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-5About this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA6About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Diabetes MellitusReads 1 of these genesGATA6About this report →
- Thyroid CancerReads 1 of these genesNKX2-5About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTRIM32About this report →
- Epilepsy (Full Panel)Reads 2 of these genesSLC6A1SYNGAP1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesCOG6About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesUQCC2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTBX1About this report →
Lue Postaxial polydactyly-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test89 geeniä, jotka liittyvät piirteeseen Postaxial polydactyly
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Postaxial polydactyly esiintyy. Useimmilla, joilla on tämä piirre, ei ole mitään näistä sairauksista, eikä tämän listan geeni kerro mitään kenenkään omasta genomista.
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| ARL6ARF like GTPase 6 | Aina | 3 sairaudessa |
| B9D2B9 domain containing 2 | Aina | 1 sairaudessa |
| BBS7Bardet-Biedl syndrome 7 | Aina | 2 sairaudessa |
| BBS9Bardet-Biedl syndrome 9 | Aina | 2 sairaudessa |
| CILK1ciliogenesis associated kinase 1 | Aina | 1 sairaudessa |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Aina | 1 sairaudessa |
| IFT52intraflagellar transport 52 | Aina | 1 sairaudessa |
| IFT74intraflagellar transport 74 | Aina | 2 sairaudessa |
| INTUinturned planar cell polarity protein | Aina | 1 sairaudessa |
| MKKSMKKS centrosomal shuttling protein | Aina | 2 sairaudessa |
| MKS1MKS transition zone complex subunit 1 | Aina | 2 sairaudessa |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Aina | 1 sairaudessa |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Aina | 1 sairaudessa |
| SRSF1serine and arginine rich splicing factor 1 | Aina | 1 sairaudessa |
| TTC8tetratricopeptide repeat domain 8 | Aina | 2 sairaudessa |
| UBR5ubiquitin protein ligase E3 component n-recognin 5 | Aina | 1 sairaudessa |
| DDX59DEAD-box helicase 59 | Hyvin usein (80–99%) | 1 sairaudessa |
| GLI3GLI family zinc finger 3 | Hyvin usein (80–99%) | 1 sairaudessa |
| IFT27intraflagellar transport 27 | Hyvin usein (80–99%) | 2 sairaudessa |
| TCTN3tectonic family member 3 | Hyvin usein (80–99%) | 2 sairaudessa |
| BBIP1BBSome interacting protein 1 | Usein (30–79%) | 1 sairaudessa |
| BBS1Bardet-Biedl syndrome 1 | Usein (30–79%) | 2 sairaudessa |
| BBS10Bardet-Biedl syndrome 10 | Usein (30–79%) | 1 sairaudessa |
| BBS12Bardet-Biedl syndrome 12 | Usein (30–79%) | 1 sairaudessa |
| BBS2Bardet-Biedl syndrome 2 | Usein (30–79%) | 1 sairaudessa |
| BBS4Bardet-Biedl syndrome 4 | Usein (30–79%) | 1 sairaudessa |
| BBS5Bardet-Biedl syndrome 5 | Usein (30–79%) | 2 sairaudessa |
| CCDC28Bcoiled-coil domain containing 28B | Usein (30–79%) | 1 sairaudessa |
| CEP19centrosomal protein 19 | Usein (30–79%) | 1 sairaudessa |
| CEP290centrosomal protein 290 | Usein (30–79%) | 1 sairaudessa |
| CFAP418cilia and flagella associated protein 418 | Usein (30–79%) | 2 sairaudessa |
| CHST11carbohydrate sulfotransferase 11 | Usein (30–79%) | 1 sairaudessa |
| GDF6growth differentiation factor 6 | Usein (30–79%) | 1 sairaudessa |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Usein (30–79%) | 3 sairaudessa |
| IFT172intraflagellar transport 172 | Usein (30–79%) | 2 sairaudessa |
| IFT43intraflagellar transport 43 | Usein (30–79%) | 2 sairaudessa |
| IFT81intraflagellar transport 81 | Usein (30–79%) | 1 sairaudessa |
| LZTFL1leucine zipper transcription factor like 1 | Usein (30–79%) | 1 sairaudessa |
| NCAPG2non-SMC condensin II complex subunit G2 | Usein (30–79%) | 1 sairaudessa |
| NPHP1nephrocystin 1 | Usein (30–79%) | 1 sairaudessa |
Näytä 49 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| SCAPERS-phase cyclin A associated protein in the ER | Usein (30–79%) | 1 sairaudessa |
| SCLT1sodium channel and clathrin linker 1 | Usein (30–79%) | 1 sairaudessa |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Usein (30–79%) | 1 sairaudessa |
| TMEM231transmembrane protein 231 | Usein (30–79%) | 1 sairaudessa |
| TOGARAM1TOG array regulator of axonemal microtubules 1 | Usein (30–79%) | 1 sairaudessa |
| TRIM32tripartite motif containing 32 | Usein (30–79%) | 1 sairaudessa |
| TXNDC15thioredoxin domain containing 15 | Usein (30–79%) | 1 sairaudessa |
| USP9Xubiquitin specific peptidase 9 X-linked | Usein (30–79%) | 2 sairaudessa |
| WDPCPWD repeat containing planar cell polarity effector | Usein (30–79%) | 1 sairaudessa |
| COG6component of oligomeric golgi complex 6 | Joskus (5–29%) | 1 sairaudessa |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Joskus (5–29%) | 2 sairaudessa |
| CSPP1centrosome and spindle pole associated protein 1 | Joskus (5–29%) | 1 sairaudessa |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Joskus (5–29%) | 1 sairaudessa |
| DYNC2I2dynein 2 intermediate chain 2 | Joskus (5–29%) | 1 sairaudessa |
| EBPEBP cholestenol delta-isomerase | Joskus (5–29%) | 1 sairaudessa |
| IFT56intraflagellar transport 56 | Joskus (5–29%) | 1 sairaudessa |
| KIAA0586KIAA0586 | Joskus (5–29%) | 2 sairaudessa |
| MEGF8multiple EGF like domains 8 | Joskus (5–29%) | 1 sairaudessa |
| PIK3R2phosphoinositide-3-kinase regulatory subunit 2 | Joskus (5–29%) | 1 sairaudessa |
| PLAAphospholipase A2 activating protein | Joskus (5–29%) | 1 sairaudessa |
| PPP2R1Aprotein phosphatase 2 scaffold subunit Aalpha | Joskus (5–29%) | 2 sairaudessa |
| RBM10RNA binding motif protein 10 | Joskus (5–29%) | 2 sairaudessa |
| SETD5SET domain containing 5 | Joskus (5–29%) | 1 sairaudessa |
| SLC6A1solute carrier family 6 member 1 | Joskus (5–29%) | 1 sairaudessa |
| SLC6A11solute carrier family 6 member 11 | Joskus (5–29%) | 1 sairaudessa |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Joskus (5–29%) | 1 sairaudessa |
| TBC1D32TBC1 domain family member 32 | Joskus (5–29%) | 1 sairaudessa |
| TGFBR2transforming growth factor beta receptor 2 | Joskus (5–29%) | 1 sairaudessa |
| TMEM218transmembrane protein 218 | Joskus (5–29%) | 1 sairaudessa |
| TMEM237transmembrane protein 237 | Joskus (5–29%) | 1 sairaudessa |
| ZFXzinc finger protein X-linked | Joskus (5–29%) | 1 sairaudessa |
| CEP120centrosomal protein 120 | Ei kirjattu | 1 sairaudessa |
| CRB2crumbs cell polarity complex component 2 | Ei kirjattu | 1 sairaudessa |
| CTU2cytosolic thiouridylase subunit 2 | Ei kirjattu | 1 sairaudessa |
| DYNC2I1dynein 2 intermediate chain 1 | Ei kirjattu | 1 sairaudessa |
| GATA6GATA binding protein 6 | Ei kirjattu | 1 sairaudessa |
| GLI1GLI family zinc finger 1 | Ei kirjattu | 1 sairaudessa |
| GPC3glypican 3 | Ei kirjattu | 1 sairaudessa |
| IFT57intraflagellar transport 57 | Ei kirjattu | 1 sairaudessa |
| KIF3Bkinesin family member 3B | Ei kirjattu | 1 sairaudessa |
| LMBR1limb development membrane protein 1 | Ei kirjattu | 1 sairaudessa |
| NKX2-5NK2 homeobox 5 | Ei kirjattu | 1 sairaudessa |
| NKX2-6NK2 homeobox 6 | Ei kirjattu | 1 sairaudessa |
| RBBP8RB binding protein 8, endonuclease | Ei kirjattu | 1 sairaudessa |
| RPGRIP1LRPGRIP1 like | Ei kirjattu | 1 sairaudessa |
| TBX1T-box transcription factor 1 | Ei kirjattu | 1 sairaudessa |
| UQCC2ubiquinol-cytochrome c reductase complex assembly factor 2 | Ei kirjattu | 1 sairaudessa |
| WDR35WD repeat domain 35 | Ei kirjattu | 1 sairaudessa |
| WNT7AWnt family member 7A | Ei kirjattu | 1 sairaudessa |
Kuinka usein ilmiö esiintyy ihmisillä, joilla on jokin geenin sairauksista, niin kuin Human Phenotype Ontology sen kirjaa. Nämä sivut kuvaavat piirteitä ja niiden taustalla olevaa tutkimusta, eivätkä ne ole diagnoosi. Oireista kannattaa kysyä lääkäriltä tai geneettiseltä neuvojalta.
Tarkemmat piirteet
Laajemmat piirteet
Mistä tämä tieto tulee
- Human Phenotype Ontology, julkaisu 2026-09-01: piirre, sen nimet, määritelmä ja siihen liitetyt geenit. Lue lisää osoitteesta hpo.jax.org.
- Tietojulkaisu 2026.10.19-9814e911.
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
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