Træk
Webbed 2nd and 3rd toes
Klinisk navn: 2-3 toe syndactyly
Syndactyly with fusion of toes two and three.
Resumé
- Også kaldet
- 2-3 syndactyly of feet, 2-3 toe soft tissue syndactyly, 2-3 toes syndactyly, partial or complete syndactyly 2nd-3rd toes, Syndactyly of second and third toes, Toe syndactyly, 2-3
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Bestil min Genome Test97 gener knyttet til Webbed 2nd and 3rd toes
Ændringer i disse gener forårsager sjældne tilstande, hvor Webbed 2nd and 3rd toes ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| BBS7Bardet-Biedl syndrome 7 | Altid | I 1 tilstand |
| CLCF1cardiotrophin like cytokine factor 1 | Altid | I 1 tilstand |
| CSGALNACT1chondroitin sulfate N-acetylgalactosaminyltransferase 1 | Altid | I 1 tilstand |
| DDX11DEAD/H-box helicase 11 | Altid | I 1 tilstand |
| DHCR77-dehydrocholesterol reductase | Altid | I 2 tilstande |
| HEPHL1hephaestin like 1 | Altid | I 1 tilstand |
| IL11RAinterleukin 11 receptor subunit alpha | Altid | I 1 tilstand |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Altid | I 1 tilstand |
| JKAMPJNK1/MAPK8 associated membrane protein | Altid | I 1 tilstand |
| MEIS2Meis homeobox 2 | Altid | I 1 tilstand |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Altid | I 1 tilstand |
| RAD21RAD21 cohesin complex component | Altid | I 1 tilstand |
| RNU6ATACRNA, U6atac small nuclear | Altid | I 1 tilstand |
| SIK3SIK family kinase 3 | Altid | I 1 tilstand |
| SLC12A2solute carrier family 12 member 2 | Altid | I 1 tilstand |
| SMC3structural maintenance of chromosomes 3 | Altid | I 1 tilstand |
| TAF4TATA-box binding protein associated factor 4 | Altid | I 1 tilstand |
| TM2D3TM2 domain containing 3 | Altid | I 1 tilstand |
| TRA2Btransformer 2 beta homolog | Altid | I 1 tilstand |
| WDPCPWD repeat containing planar cell polarity effector | Altid | I 1 tilstand |
| BHLHA9basic helix-loop-helix family member a9 | Meget ofte (80–99 %) | I 1 tilstand |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Meget ofte (80–99 %) | I 2 tilstande |
| ALDH1A2aldehyde dehydrogenase 1 family member A2 | Ofte (30–79 %) | I 1 tilstand |
| BCORBCL6 corepressor | Ofte (30–79 %) | I 2 tilstande |
| CERT1ceramide transporter 1 | Ofte (30–79 %) | I 1 tilstand |
| CNTNAP1contactin associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| EBPEBP cholestenol delta-isomerase | Ofte (30–79 %) | I 2 tilstande |
| FDFT1farnesyl-diphosphate farnesyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| FGFR1fibroblast growth factor receptor 1 | Ofte (30–79 %) | I 1 tilstand |
| FGFR2fibroblast growth factor receptor 2 | Ofte (30–79 %) | I 2 tilstande |
| H4C9H4 clustered histone 9 | Ofte (30–79 %) | I 1 tilstand |
| HOXD13homeobox D13 | Ofte (30–79 %) | I 1 tilstand |
| IFT172intraflagellar transport 172 | Ofte (30–79 %) | I 1 tilstand |
| IFT43intraflagellar transport 43 | Ofte (30–79 %) | I 2 tilstande |
| KMT2Alysine methyltransferase 2A | Ofte (30–79 %) | I 1 tilstand |
| KMT2Blysine methyltransferase 2B | Ofte (30–79 %) | I 1 tilstand |
| LRRC8Cleucine rich repeat containing 8 VRAC subunit C | Ofte (30–79 %) | I 1 tilstand |
| MED25mediator complex subunit 25 | Ofte (30–79 %) | I 2 tilstande |
| MEF2Cmyocyte enhancer factor 2C | Ofte (30–79 %) | I 1 tilstand |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Ofte (30–79 %) | I 2 tilstande |
Vis 57 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| MYRFmyelin regulatory factor | Ofte (30–79 %) | I 1 tilstand |
| NBNnibrin | Ofte (30–79 %) | I 1 tilstand |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Ofte (30–79 %) | I 1 tilstand |
| PDE6Dphosphodiesterase 6D | Ofte (30–79 %) | I 1 tilstand |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Ofte (30–79 %) | I 1 tilstand |
| RALARAS like proto-oncogene A | Ofte (30–79 %) | I 1 tilstand |
| SCARF2scavenger receptor class F member 2 | Ofte (30–79 %) | I 1 tilstand |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Ofte (30–79 %) | I 1 tilstand |
| SHMT2serine hydroxymethyltransferase 2 | Ofte (30–79 %) | I 1 tilstand |
| SOX5SRY-box transcription factor 5 | Ofte (30–79 %) | I 1 tilstand |
| TRIOtrio Rho guanine nucleotide exchange factor | Ofte (30–79 %) | I 2 tilstande |
| TRMT5tRNA methyltransferase 5 | Ofte (30–79 %) | I 1 tilstand |
| AP1G1adaptor related protein complex 1 subunit gamma 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ARMC9armadillo repeat containing 9 | Nogle gange (5–29 %) | I 1 tilstand |
| CDC45cell division cycle 45 | Nogle gange (5–29 %) | I 1 tilstand |
| CNOT2CCR4-NOT transcription complex subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| CTCFCCCTC-binding factor | Nogle gange (5–29 %) | I 1 tilstand |
| DDX6DEAD-box helicase 6 | Nogle gange (5–29 %) | I 1 tilstand |
| FBXW11F-box and WD repeat domain containing 11 | Nogle gange (5–29 %) | I 1 tilstand |
| JARID2jumonji and AT-rich interaction domain containing 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Nogle gange (5–29 %) | I 1 tilstand |
| KDM5Alysine demethylase 5A | Nogle gange (5–29 %) | I 1 tilstand |
| MAB21L2mab-21 like 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MAPRE2microtubule associated protein RP/EB family member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| PHIPPHIP subunit of CUL4-Ring ligase complex | Nogle gange (5–29 %) | I 1 tilstand |
| PLAAT3phospholipase A and acyltransferase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| POLR3ARNA polymerase III subunit A | Nogle gange (5–29 %) | I 1 tilstand |
| PUF60poly(U) binding splicing factor 60 | Nogle gange (5–29 %) | I 1 tilstand |
| RAI1retinoic acid induced 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RBPJrecombination signal binding protein for immunoglobulin kappa J region | Nogle gange (5–29 %) | I 1 tilstand |
| SATB1SATB homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| STAG1STAG1 cohesin complex component | Nogle gange (5–29 %) | I 1 tilstand |
| SYT1synaptotagmin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TTI2TELO2 interacting protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| UBE2Aubiquitin conjugating enzyme E2 A | Nogle gange (5–29 %) | I 1 tilstand |
| ADNPactivity dependent neuroprotector homeobox | Sjældent (1–4%) | I 1 tilstand |
| APC2APC regulator of Wnt signaling pathway 2 | Sjældent (1–4%) | I 1 tilstand |
| MAN1B1mannosidase alpha class 1B member 1 | Sjældent (1–4%) | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Sjældent (1–4%) | I 1 tilstand |
| TBCKTBC1 domain containing kinase | Sjældent (1–4%) | I 1 tilstand |
| ARCN1archain 1 coat protein complex I subunit delta | Ikke registreret | I 1 tilstand |
| BMP2bone morphogenetic protein 2 | Ikke registreret | I 1 tilstand |
| BMPR1Bbone morphogenetic protein receptor type 1B | Ikke registreret | I 1 tilstand |
| CEP55centrosomal protein 55 | Ikke registreret | I 1 tilstand |
| GDF5growth differentiation factor 5 | Ikke registreret | I 1 tilstand |
| KCTD1potassium channel tetramerization domain containing 1 | Ikke registreret | I 1 tilstand |
| LMBR1limb development membrane protein 1 | Ikke registreret | I 1 tilstand |
| NIPBLNIPBL cohesin loading factor | Ikke registreret | I 1 tilstand |
| NOGnoggin | Ikke registreret | I 1 tilstand |
| SALL1spalt like transcription factor 1 | Ikke registreret | I 1 tilstand |
| SLC12A6solute carrier family 12 member 6 | Ikke registreret | I 1 tilstand |
| SMAD4SMAD family member 4 | Ikke registreret | I 1 tilstand |
| TBX15T-box transcription factor 15 | Ikke registreret | I 1 tilstand |
| TP63tumor protein p63 | Ikke registreret | I 1 tilstand |
| TXNL4Athioredoxin like 4A | Ikke registreret | I 1 tilstand |
| ZMIZ1zinc finger MIZ-type containing 1 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.16-c6eea6bf.
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