Tunnus
Feet or buttocks of fetus positioned near opening of uterus
Kliiniline nimetus: Breech presentation
A position of the fetus at delivery in which the fetus enters the birth canal with the buttocks or feet first.
Kokkuvõte
- Teised nimetused
- Breech presentation at birth, Feet or buttocks of foetus positioned near opening of uterus
- Kehasüsteem
- Abnormality of prenatal development or birth
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Feet or buttocks of fetus positioned near opening of uterus, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test60 geeni on seotud tunnusega Feet or buttocks of fetus positioned near opening of uterus
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Feet or buttocks of fetus positioned near opening of uterus. 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 |
|---|---|---|
| ACTA1actin alpha 1, skeletal muscle | Alati | Esineb 3 haiguses |
| ACY1aminoacylase 1 | Alati | Esineb 1 haiguses |
| ASH1LASH1 like histone lysine methyltransferase | Alati | Esineb 1 haiguses |
| ASXL3ASXL transcriptional regulator 3 | Alati | Esineb 1 haiguses |
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | Alati | Esineb 1 haiguses |
| FGFR3fibroblast growth factor receptor 3 | Alati | Esineb 2 haiguses |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Alati | Esineb 1 haiguses |
| KDM6Blysine demethylase 6B | Alati | Esineb 1 haiguses |
| PTPN23protein tyrosine phosphatase non-receptor type 23 | Alati | Esineb 1 haiguses |
| RYR1ryanodine receptor 1 | Alati | Esineb 1 haiguses |
| SONSON DNA and RNA binding protein | Alati | Esineb 1 haiguses |
| UBAP2Lubiquitin associated protein 2 like | Alati | Esineb 1 haiguses |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Alati | Esineb 1 haiguses |
| UQCC2ubiquinol-cytochrome c reductase complex assembly factor 2 | Alati | Esineb 1 haiguses |
| CFL2cofilin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CHST3carbohydrate sulfotransferase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DSTdystonin | Sageli (30–79%) | Esineb 1 haiguses |
| DTYMKdeoxythymidylate kinase | Sageli (30–79%) | Esineb 1 haiguses |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Sageli (30–79%) | Esineb 1 haiguses |
| KLHL40kelch like family member 40 | Sageli (30–79%) | Esineb 1 haiguses |
| KLHL41kelch like family member 41 | Sageli (30–79%) | Esineb 3 haiguses |
| LMOD3leiomodin 3 | Sageli (30–79%) | Esineb 2 haiguses |
| NEBnebulin | Sageli (30–79%) | Esineb 2 haiguses |
| OPA1OPA1 mitochondrial dynamin like GTPase | Sageli (30–79%) | Esineb 1 haiguses |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Sageli (30–79%) | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Sageli (30–79%) | Esineb 1 haiguses |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Sageli (30–79%) | Esineb 2 haiguses |
| SHPKsedoheptulokinase | Sageli (30–79%) | Esineb 1 haiguses |
| VARS1valyl-tRNA synthetase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| COL1A1collagen type I alpha 1 chain | Mõnikord (5–29%) | Esineb 2 haiguses |
| COL1A2collagen type I alpha 2 chain | Mõnikord (5–29%) | Esineb 2 haiguses |
| COL25A1collagen type XXV alpha 1 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERGIC1endoplasmic reticulum-golgi intermediate compartment 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KBTBD13kelch repeat and BTB domain containing 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KDM3Blysine demethylase 3B | Mõnikord (5–29%) | Esineb 1 haiguses |
| LTBP4latent transforming growth factor beta binding protein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAGEL2MAGE family member L2 | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 20 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| MKRN3makorin ring finger protein 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MYPNmyopalladin | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPAP1nuclear pore associated protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PWAR1Prader Willi/Angelman region RNA 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU4ATACRNA, U4atac small nuclear | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCYL2SCY1 like pseudokinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TPM2tropomyosin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TPM3tropomyosin 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZNF699zinc finger protein 699 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRTAPcartilage associated protein | Pole registreeritud | Esineb 1 haiguses |
| DHCR77-dehydrocholesterol reductase | Pole registreeritud | Esineb 1 haiguses |
| MKS1MKS transition zone complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| MYH3myosin heavy chain 3 | Pole registreeritud | Esineb 1 haiguses |
| ORC1origin recognition complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| PEX1peroxisomal biogenesis factor 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC26A2solute carrier family 26 member 2 | 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