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Egenskap
Inward turned thumb
Klinisk navn: Adducted thumb
In the resting position, the tip of the thumb is on, or near, the palm, close to the base of the fourth or fifth finger.
Sammendrag
- Også kalt
- Adducted thumbs, Thumb-in-palm deformity, Thumb-in-palm pattern
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/adducted-thumb.json"
page <- fromJSON(url)
page$trait$nameInward turned thumbHP:0001181
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Les genene knyttet til Inward turned thumb, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test49 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.
- Congenital MyopathiesReads 6 of these genesTPM2ACTA1KLHL40KLHL41LMOD3NEBAbout this report →
- Alkuraya-Kucinskas SyndromeReads 1 of these genesBLTP1About this report →
- Basilicata-Akhtar SyndromeReads 1 of these genesMSL3About this report →
- Catel-Manzke SyndromeReads 1 of these genesTGDSAbout this report →
Show 45 more reports
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
- KCNH1-Related DisorderReads 1 of these genesKCNH1About this report →
- L1 SyndromeReads 1 of these genesL1CAMAbout this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- NDE1-Related MicrolissencephalyReads 1 of these genesNDE1About this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- Stüve-Wiedemann SyndromeReads 1 of these genesLIFRAbout this report →
- Turnpenny-Fry SyndromeReads 1 of these genesPCGF2About this report →
- Congenital Muscular DystrophiesReads 5 of these genesCOL12A1COL6A1COL6A2COL6A3CRPPAAbout this report →
- Congenital Disorders of GlycosylationReads 9 of these genesCOG7DSERFT1B3GALT6PIGYALG13About this report →
- Ehlers-Danlos SyndromeReads 4 of these genesDSEB3GALT6COL12A1CHST14About this report →
- Cutis LaxaReads 3 of these genesALDH18A1ELNFBLN5About this report →
- Marfan Like SyndromesReads 2 of these genesFBN1FBN2About this report →
- Lissencephaly Spectrum DisordersReads 3 of these genesKATNB1NDE1RELNAbout this report →
- Monogenic Precocious PubertyReads 1 of these genesDLK1About this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesCOL6A1COL6A2COL6A3About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesDSTCRLF1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Nephrotic SyndromeReads 2 of these genesNUP107NUP133About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesAP4M1ALDH18A1L1CAMAbout this report →
- Inherited Neurodegenerative DisordersReads 7 of these genesNALCNSYNE1AP4M1ALDH18A1BICD2L1CAMAbout this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesPHGDHAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesTOR1ACOL6A3About this report →
- Epilepsy (Full Panel)Reads 4 of these genesALG13GNB1RELNZEB2About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesSYNE1STUB1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesDSTBICD2FBLN5CRLF1About this report →
- Intellectual DisabilityReads 4 of these genesCREBBPGNB1ZEB2EP300About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesANKLE2About this report →
- Epidermolysis BullosaReads 1 of these genesDSTAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGYAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesEXOSC9About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesRNU4-2About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesERCC1About this report →
- Spinal Muscular AtrophyReads 1 of these genesBICD2About this report →
- Inherited ThrombocytopeniasReads 1 of these genesRBM8AAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesSTUB1About this report →
- DNA Repair DiseaseReads 1 of these genesERCC1About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Dilated CardiomyopathyReads 1 of these genesSYNE1About this report →
- Female InfertilityReads 1 of these genesNUP107About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesFBLN5About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNCF1About this report →
Les genene knyttet til Inward turned thumb, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test105 gener knyttet til Inward turned thumb
Endringer i disse genene forårsaker sjeldne tilstander der Inward turned thumb forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| CHASERRCHD2 adjacent suppressive regulatory RNA | Alltid | I 1 tilstand |
| COG7component of oligomeric golgi complex 7 | Alltid | I 2 tilstander |
| DSEdermatan sulfate epimerase | Alltid | I 1 tilstand |
| DSTdystonin | Alltid | I 1 tilstand |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Alltid | I 1 tilstand |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Alltid | I 1 tilstand |
| MOCS3molybdenum cofactor synthesis 3 | Alltid | I 1 tilstand |
| MYH3myosin heavy chain 3 | Alltid | I 4 tilstander |
| NALCNsodium leak channel, non-selective | Alltid | I 4 tilstander |
| RBM8ARNA binding motif protein 8A | Alltid | I 2 tilstander |
| RFT1RFT1 glycolipid translocator homolog | Alltid | I 1 tilstand |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Alltid | I 2 tilstander |
| TOR1Atorsin family 1 member A | Alltid | I 1 tilstand |
| ANKLE2ankyrin repeat and LEM domain containing 2 | Svært ofte (80–99 %) | I 1 tilstand |
| AP4M1adaptor related protein complex 4 subunit mu 1 | Svært ofte (80–99 %) | I 1 tilstand |
| FBN1fibrillin 1 | Svært ofte (80–99 %) | I 1 tilstand |
| MYBPC1myosin binding protein C1 | Svært ofte (80–99 %) | I 1 tilstand |
| TNNI2troponin I2, fast skeletal type | Svært ofte (80–99 %) | I 2 tilstander |
| TNNT3troponin T3, fast skeletal type | Svært ofte (80–99 %) | I 3 tilstander |
| TPM2tropomyosin 2 | Svært ofte (80–99 %) | I 3 tilstander |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Ofte (30–79 %) | I 3 tilstander |
| B3GALT6beta-1,3-galactosyltransferase 6 | Ofte (30–79 %) | I 1 tilstand |
| BICD2BICD cargo adaptor 2 | Ofte (30–79 %) | I 1 tilstand |
| CHST11carbohydrate sulfotransferase 11 | Ofte (30–79 %) | I 1 tilstand |
| COL12A1collagen type XII alpha 1 chain | Ofte (30–79 %) | I 2 tilstander |
| COL6A1collagen type VI alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COL6A2collagen type VI alpha 2 chain | Ofte (30–79 %) | I 2 tilstander |
| COL6A3collagen type VI alpha 3 chain | Ofte (30–79 %) | I 1 tilstand |
| DPH2diphthamide biosynthesis 2 | Ofte (30–79 %) | I 1 tilstand |
| EXOSC9exosome component 9 | Ofte (30–79 %) | I 1 tilstand |
| FBN2fibrillin 2 | Ofte (30–79 %) | I 1 tilstand |
| L1CAML1 cell adhesion molecule | Ofte (30–79 %) | I 4 tilstander |
| NEK9NIMA related kinase 9 | Ofte (30–79 %) | I 1 tilstand |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Ofte (30–79 %) | I 1 tilstand |
| SLC35B2solute carrier family 35 member B2 | Ofte (30–79 %) | I 1 tilstand |
| SLC9A6solute carrier family 9 member A6 | Ofte (30–79 %) | I 2 tilstander |
| STUB1STIP1 homology and U-box containing protein 1 | Ofte (30–79 %) | I 1 tilstand |
| ACTA1actin alpha 1, skeletal muscle | Noen ganger (5–29 %) | I 1 tilstand |
| ADGRG6adhesion G protein-coupled receptor G6 | Noen ganger (5–29 %) | I 1 tilstand |
| ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunit | Noen ganger (5–29 %) | I 1 tilstand |
Vis 65 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Noen ganger (5–29 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Noen ganger (5–29 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| CREBBPCREB binding lysine acetyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| DLK1delta like non-canonical Notch ligand 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Noen ganger (5–29 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Noen ganger (5–29 %) | I 1 tilstand |
| ELNelastin | Noen ganger (5–29 %) | I 2 tilstander |
| EPB41L1erythrocyte membrane protein band 4.1 like 1 | Noen ganger (5–29 %) | I 1 tilstand |
| FBLN5fibulin 5 | Noen ganger (5–29 %) | I 1 tilstand |
| FILIP1filamin A interacting protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Noen ganger (5–29 %) | I 1 tilstand |
| GNB1G protein subunit beta 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GON7GON7 subunit of KEOPS complex | Noen ganger (5–29 %) | I 1 tilstand |
| GPKOWG-patch domain and KOW motifs | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2Igeneral transcription factor IIi | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KATNB1katanin regulatory subunit B1 | Noen ganger (5–29 %) | I 1 tilstand |
| KLHL40kelch like family member 40 | Noen ganger (5–29 %) | I 1 tilstand |
| KLHL41kelch like family member 41 | Noen ganger (5–29 %) | I 1 tilstand |
| LAGE3L antigen family member 3 | Noen ganger (5–29 %) | I 1 tilstand |
| LIMK1LIM domain kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| LMOD3leiomodin 3 | Noen ganger (5–29 %) | I 1 tilstand |
| MED25mediator complex subunit 25 | Noen ganger (5–29 %) | I 1 tilstand |
| MEG3maternally expressed 3 | Noen ganger (5–29 %) | I 1 tilstand |
| METTL27methyltransferase like 27 | Noen ganger (5–29 %) | I 1 tilstand |
| MSL3MSL complex subunit 3 | Noen ganger (5–29 %) | I 1 tilstand |
| MYL11myosin light chain 11 | Noen ganger (5–29 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| NDE1nudE neurodevelopment protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| NEBnebulin | Noen ganger (5–29 %) | I 2 tilstander |
| NUP107nucleoporin 107 | Noen ganger (5–29 %) | I 1 tilstand |
| NUP133nucleoporin 133 | Noen ganger (5–29 %) | I 1 tilstand |
| OSGEPO-sialoglycoprotein endopeptidase | Noen ganger (5–29 %) | I 1 tilstand |
| PHGDHphosphoglycerate dehydrogenase | Noen ganger (5–29 %) | I 2 tilstander |
| RELNreelin | Noen ganger (5–29 %) | I 1 tilstand |
| RFC2replication factor C subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| RTL1retrotransposon Gag like 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SHMT2serine hydroxymethyltransferase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| STX1Asyntaxin 1A | Noen ganger (5–29 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TGDSTDP-glucose 4,6-dehydratase | Noen ganger (5–29 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Noen ganger (5–29 %) | I 1 tilstand |
| TP53RKTP53 regulating kinase | Noen ganger (5–29 %) | I 1 tilstand |
| TPRKBTP53RK binding protein | Noen ganger (5–29 %) | I 1 tilstand |
| VPS37DVPS37D subunit of ESCRT-I | Noen ganger (5–29 %) | I 1 tilstand |
| WDR4WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| WDR73WD repeat domain 73 | Noen ganger (5–29 %) | I 1 tilstand |
| YRDCyrdC N6-threonylcarbamoyltransferase domain containing | Noen ganger (5–29 %) | I 1 tilstand |
| ZEB2zinc finger E-box binding homeobox 2 | Noen ganger (5–29 %) | I 2 tilstander |
| EP300EP300 lysine acetyltransferase | Sjelden (1–4%) | I 1 tilstand |
| RNU4-2RNA, U4 small nuclear 2 | Sjelden (1–4%) | I 1 tilstand |
| SMPD4sphingomyelin phosphodiesterase 4 | Sjelden (1–4%) | I 1 tilstand |
| ALG3ALG3 alpha-1,3- mannosyltransferase | Ikke registrert | I 1 tilstand |
| ATAD1ATPase family AAA domain containing 1 | Ikke registrert | I 1 tilstand |
| BLTP1bridge-like lipid transfer protein family member 1 | Ikke registrert | I 1 tilstand |
| CHST14carbohydrate sulfotransferase 14 | Ikke registrert | I 1 tilstand |
| CRLF1cytokine receptor like factor 1 | Ikke registrert | I 1 tilstand |
| CRPPACDP-L-ribitol pyrophosphorylase A | Ikke registrert | I 1 tilstand |
| ECEL1endothelin converting enzyme like 1 | Ikke registrert | I 1 tilstand |
| LIFRLIF receptor subunit alpha | Ikke registrert | I 1 tilstand |
| PCGF2polycomb group ring finger 2 | Ikke registrert | I 1 tilstand |
| TAPT1transmembrane anterior posterior transformation 1 | Ikke registrert | I 1 tilstand |
| TDO2tryptophan 2,3-dioxygenase | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
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