Tunnus
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.
Kokkuvõte
- Teised nimetused
- Polydactyly, postaxial, Postaxial hexadactyly
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Postaxial polydactyly, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test89 geeni on seotud tunnusega Postaxial polydactyly
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Postaxial polydactyly. 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 |
|---|---|---|
| ARL6ARF like GTPase 6 | Alati | Esineb 3 haiguses |
| B9D2B9 domain containing 2 | Alati | Esineb 1 haiguses |
| BBS7Bardet-Biedl syndrome 7 | Alati | Esineb 2 haiguses |
| BBS9Bardet-Biedl syndrome 9 | Alati | Esineb 2 haiguses |
| CILK1ciliogenesis associated kinase 1 | Alati | Esineb 1 haiguses |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Alati | Esineb 1 haiguses |
| IFT52intraflagellar transport 52 | Alati | Esineb 1 haiguses |
| IFT74intraflagellar transport 74 | Alati | Esineb 2 haiguses |
| INTUinturned planar cell polarity protein | Alati | Esineb 1 haiguses |
| MKKSMKKS centrosomal shuttling protein | Alati | Esineb 2 haiguses |
| MKS1MKS transition zone complex subunit 1 | Alati | Esineb 2 haiguses |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Alati | Esineb 1 haiguses |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Alati | Esineb 1 haiguses |
| SRSF1serine and arginine rich splicing factor 1 | Alati | Esineb 1 haiguses |
| TTC8tetratricopeptide repeat domain 8 | Alati | Esineb 2 haiguses |
| UBR5ubiquitin protein ligase E3 component n-recognin 5 | Alati | Esineb 1 haiguses |
| DDX59DEAD-box helicase 59 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GLI3GLI family zinc finger 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| IFT27intraflagellar transport 27 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TCTN3tectonic family member 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| BBIP1BBSome interacting protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| BBS1Bardet-Biedl syndrome 1 | Sageli (30–79%) | Esineb 2 haiguses |
| BBS10Bardet-Biedl syndrome 10 | Sageli (30–79%) | Esineb 1 haiguses |
| BBS12Bardet-Biedl syndrome 12 | Sageli (30–79%) | Esineb 1 haiguses |
| BBS2Bardet-Biedl syndrome 2 | Sageli (30–79%) | Esineb 1 haiguses |
| BBS4Bardet-Biedl syndrome 4 | Sageli (30–79%) | Esineb 1 haiguses |
| BBS5Bardet-Biedl syndrome 5 | Sageli (30–79%) | Esineb 2 haiguses |
| CCDC28Bcoiled-coil domain containing 28B | Sageli (30–79%) | Esineb 1 haiguses |
| CEP19centrosomal protein 19 | Sageli (30–79%) | Esineb 1 haiguses |
| CEP290centrosomal protein 290 | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP418cilia and flagella associated protein 418 | Sageli (30–79%) | Esineb 2 haiguses |
| CHST11carbohydrate sulfotransferase 11 | Sageli (30–79%) | Esineb 1 haiguses |
| GDF6growth differentiation factor 6 | Sageli (30–79%) | Esineb 1 haiguses |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Sageli (30–79%) | Esineb 3 haiguses |
| IFT172intraflagellar transport 172 | Sageli (30–79%) | Esineb 2 haiguses |
| IFT43intraflagellar transport 43 | Sageli (30–79%) | Esineb 2 haiguses |
| IFT81intraflagellar transport 81 | Sageli (30–79%) | Esineb 1 haiguses |
| LZTFL1leucine zipper transcription factor like 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NCAPG2non-SMC condensin II complex subunit G2 | Sageli (30–79%) | Esineb 1 haiguses |
| NPHP1nephrocystin 1 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 49 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SCAPERS-phase cyclin A associated protein in the ER | Sageli (30–79%) | Esineb 1 haiguses |
| SCLT1sodium channel and clathrin linker 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Sageli (30–79%) | Esineb 1 haiguses |
| TMEM231transmembrane protein 231 | Sageli (30–79%) | Esineb 1 haiguses |
| TOGARAM1TOG array regulator of axonemal microtubules 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TRIM32tripartite motif containing 32 | Sageli (30–79%) | Esineb 1 haiguses |
| TXNDC15thioredoxin domain containing 15 | Sageli (30–79%) | Esineb 1 haiguses |
| USP9Xubiquitin specific peptidase 9 X-linked | Sageli (30–79%) | Esineb 2 haiguses |
| WDPCPWD repeat containing planar cell polarity effector | Sageli (30–79%) | Esineb 1 haiguses |
| COG6component of oligomeric golgi complex 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| CSPP1centrosome and spindle pole associated protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYNC2I2dynein 2 intermediate chain 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EBPEBP cholestenol delta-isomerase | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFT56intraflagellar transport 56 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIAA0586KIAA0586 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MEGF8multiple EGF like domains 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIK3R2phosphoinositide-3-kinase regulatory subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PLAAphospholipase A2 activating protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP2R1Aprotein phosphatase 2 scaffold subunit Aalpha | Mõnikord (5–29%) | Esineb 2 haiguses |
| RBM10RNA binding motif protein 10 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SETD5SET domain containing 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC6A1solute carrier family 6 member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC6A11solute carrier family 6 member 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBC1D32TBC1 domain family member 32 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGFBR2transforming growth factor beta receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TMEM218transmembrane protein 218 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TMEM237transmembrane protein 237 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZFXzinc finger protein X-linked | Mõnikord (5–29%) | Esineb 1 haiguses |
| CEP120centrosomal protein 120 | Pole registreeritud | Esineb 1 haiguses |
| CRB2crumbs cell polarity complex component 2 | Pole registreeritud | Esineb 1 haiguses |
| CTU2cytosolic thiouridylase subunit 2 | Pole registreeritud | Esineb 1 haiguses |
| DYNC2I1dynein 2 intermediate chain 1 | Pole registreeritud | Esineb 1 haiguses |
| GATA6GATA binding protein 6 | Pole registreeritud | Esineb 1 haiguses |
| GLI1GLI family zinc finger 1 | Pole registreeritud | Esineb 1 haiguses |
| GPC3glypican 3 | Pole registreeritud | Esineb 1 haiguses |
| IFT57intraflagellar transport 57 | Pole registreeritud | Esineb 1 haiguses |
| KIF3Bkinesin family member 3B | Pole registreeritud | Esineb 1 haiguses |
| LMBR1limb development membrane protein 1 | Pole registreeritud | Esineb 1 haiguses |
| NKX2-5NK2 homeobox 5 | Pole registreeritud | Esineb 1 haiguses |
| NKX2-6NK2 homeobox 6 | Pole registreeritud | Esineb 1 haiguses |
| RBBP8RB binding protein 8, endonuclease | Pole registreeritud | Esineb 1 haiguses |
| RPGRIP1LRPGRIP1 like | Pole registreeritud | Esineb 1 haiguses |
| TBX1T-box transcription factor 1 | Pole registreeritud | Esineb 1 haiguses |
| UQCC2ubiquinol-cytochrome c reductase complex assembly factor 2 | Pole registreeritud | Esineb 1 haiguses |
| WDR35WD repeat domain 35 | Pole registreeritud | Esineb 1 haiguses |
| WNT7AWnt family member 7A | 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.
Kitsamad tunnused
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.
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast