Tunnus
Gap between 1st and 2nd toes
Kliiniline nimetus: Sandal gap
A widely spaced gap between the first toe (the great toe) and the second toe.
Kokkuvõte
- Teised nimetused
- Gap between first and second toe, Increased space between first and second toes, Sandal gap between first and second toes, Wide space between 1st, 2nd toes, Wide space between first and second toes, Wide-spaced big toe, Widely spaced 1st-2nd toes, Widely spaced first and second toes, Widened gap 1st-2nd toes, Widened gap first and second toe, Space between great toe and second toe
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Gap between 1st and 2nd toes, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test112 geeni on seotud tunnusega Gap between 1st and 2nd toes
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Gap between 1st and 2nd toes. 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 |
|---|---|---|
| ALG12ALG12 alpha-1,6-mannosyltransferase | Alati | Esineb 2 haiguses |
| ARID1AAT-rich interaction domain 1A | Alati | Esineb 1 haiguses |
| CILK1ciliogenesis associated kinase 1 | Alati | Esineb 2 haiguses |
| DCPSdecapping enzyme, scavenger | Alati | Esineb 1 haiguses |
| DMRT2doublesex and mab-3 related transcription factor 2 | Alati | Esineb 1 haiguses |
| DSPdesmoplakin | Alati | Esineb 1 haiguses |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Alati | Esineb 1 haiguses |
| JKAMPJNK1/MAPK8 associated membrane protein | Alati | Esineb 1 haiguses |
| KDM2Blysine demethylase 2B | Alati | Esineb 1 haiguses |
| KDM6Blysine demethylase 6B | Alati | Esineb 1 haiguses |
| MBD5methyl-CpG binding domain protein 5 | Alati | Esineb 2 haiguses |
| MED16mediator complex subunit 16 | Alati | Esineb 1 haiguses |
| MEIS2Meis homeobox 2 | Alati | Esineb 1 haiguses |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Alati | Esineb 2 haiguses |
| ATRATR checkpoint kinase | Väga sageli (80–99%) | Esineb 2 haiguses |
| ATRIPATR interacting protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CENPEcentromere protein E | Väga sageli (80–99%) | Esineb 1 haiguses |
| CEP152centrosomal protein 152 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CEP295centrosomal protein 295 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CEP63centrosomal protein 63 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CPAPcentrosome assembly and centriole elongation protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CUL4Bcullin 4B | Väga sageli (80–99%) | Esineb 2 haiguses |
| DNA2DNA replication helicase/nuclease 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FLNAfilamin A | Väga sageli (80–99%) | Esineb 2 haiguses |
| NINninein | Väga sageli (80–99%) | Esineb 1 haiguses |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP85nucleoporin 85 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PCNTpericentrin | Väga sageli (80–99%) | Esineb 1 haiguses |
| PLK4polo like kinase 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RBBP8RB binding protein 8, endonuclease | Väga sageli (80–99%) | Esineb 1 haiguses |
| SMOC1SPARC related modular calcium binding 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TRAIPTRAF interacting protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| VPS13Bvacuolar protein sorting 13 homolog B | Väga sageli (80–99%) | Esineb 1 haiguses |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| BCORBCL6 corepressor | Sageli (30–79%) | Esineb 1 haiguses |
| BMP2bone morphogenetic protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CHST11carbohydrate sulfotransferase 11 | Sageli (30–79%) | Esineb 1 haiguses |
| CHST3carbohydrate sulfotransferase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| CREBBPCREB binding lysine acetyltransferase | Sageli (30–79%) | Esineb 2 haiguses |
| CTCFCCCTC-binding factor | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 72 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| DDX59DEAD-box helicase 59 | Sageli (30–79%) | Esineb 1 haiguses |
| EFNB1ephrin B1 | Sageli (30–79%) | Esineb 1 haiguses |
| EP300EP300 lysine acetyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| H4C9H4 clustered histone 9 | Sageli (30–79%) | Esineb 1 haiguses |
| IFT43intraflagellar transport 43 | Sageli (30–79%) | Esineb 1 haiguses |
| LTBP4latent transforming growth factor beta binding protein 4 | Sageli (30–79%) | Esineb 1 haiguses |
| NBASNBAS subunit of NRZ tethering complex | Sageli (30–79%) | Esineb 1 haiguses |
| NBNnibrin | Sageli (30–79%) | Esineb 1 haiguses |
| NXNnucleoredoxin | Sageli (30–79%) | Esineb 2 haiguses |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sageli (30–79%) | Esineb 2 haiguses |
| PPFIA3PPFI scaffold protein A3 | Sageli (30–79%) | Esineb 1 haiguses |
| PRKG2protein kinase cGMP-dependent 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SALL4spalt like transcription factor 4 | Sageli (30–79%) | Esineb 2 haiguses |
| SETD5SET domain containing 5 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC26A2solute carrier family 26 member 2 | Sageli (30–79%) | Esineb 3 haiguses |
| SMARCD2SWI/SNF related BAF chromatin remodeling complex subunit D2 | Sageli (30–79%) | Esineb 1 haiguses |
| SVILsupervillin | Sageli (30–79%) | Esineb 1 haiguses |
| TBC1D32TBC1 domain family member 32 | Sageli (30–79%) | Esineb 1 haiguses |
| TCF20transcription factor 20 | Sageli (30–79%) | Esineb 1 haiguses |
| ABL1ABL proto-oncogene 1, non-receptor tyrosine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ADNPactivity dependent neuroprotector homeobox | Mõnikord (5–29%) | Esineb 2 haiguses |
| AEBP1AE binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARID1BAT-rich interaction domain 1B | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCL11ABCL11 transcription factor A | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCRBCR activator of RhoGEF and GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BPTFbromodomain PHD finger transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL11A2collagen type XI alpha 2 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL1A2collagen type I alpha 2 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| COX7Bcytochrome c oxidase subunit 7B | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRKLCRK like proto-oncogene, adaptor protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Mõnikord (5–29%) | Esineb 1 haiguses |
| EBF3EBF transcription factor 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBXO11F-box protein 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBXW11F-box and WD repeat domain containing 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HEATR3HEAT repeat containing 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KAT6Alysine acetyltransferase 6A | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAN2C1mannosidase alpha class 2C member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAPK1mitogen-activated protein kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MTX2metaxin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| NSD1nuclear receptor binding SET domain protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAI1retinoic acid induced 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RELREL proto-oncogene, NF-kB subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| RFX7regulatory factor X7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RHOAras homolog family member A | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU5B-1RNA, U5B small nuclear 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ROR2ROR family WNT receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SATB1SATB homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SETBP1SET binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC32A1solute carrier family 32 member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SUZ12SUZ12 polycomb repressive complex 2 subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBX4T-box transcription factor 4 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TRAF7TNF receptor associated factor 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIOtrio Rho guanine nucleotide exchange factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| WBP4WW domain binding protein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| XPO1exportin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| YY1YY1 transcription factor | Mõnikord (5–29%) | Esineb 2 haiguses |
| CANT1calcium activated nucleotidase 1 | Pole registreeritud | Esineb 1 haiguses |
| FLNBfilamin B | Pole registreeritud | Esineb 1 haiguses |
| GALNT2polypeptide N-acetylgalactosaminyltransferase 2 | Pole registreeritud | Esineb 1 haiguses |
| GMNNgeminin DNA replication inhibitor | Pole registreeritud | Esineb 1 haiguses |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Pole registreeritud | Esineb 1 haiguses |
| IFT52intraflagellar transport 52 | Pole registreeritud | Esineb 1 haiguses |
| IFT57intraflagellar transport 57 | Pole registreeritud | Esineb 1 haiguses |
| IGF1Rinsulin like growth factor 1 receptor | Pole registreeritud | Esineb 1 haiguses |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Pole registreeritud | Esineb 1 haiguses |
| TNNT3troponin T3, fast skeletal type | Pole registreeritud | Esineb 1 haiguses |
| TRIP12thyroid hormone receptor interactor 12 | 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 2026.10.16-c6eea6bf.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast