Tunnus
Wet cough
Kliiniline nimetus: Productive cough
A cough that produces phlegm or mucus.
Kokkuvõte
- Teised nimetused
- Cough with mucus production
- Kehasüsteem
- Abnormality of the respiratory system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Wet cough, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test73 geeni on seotud tunnusega Wet cough
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Wet cough. 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 |
|---|---|---|
| BRWD1bromodomain and WD repeat domain containing 1 | Alati | Esineb 2 haiguses |
| CFAP300cilia and flagella associated protein 300 | Alati | Esineb 2 haiguses |
| CFAP54cilia and flagella associated protein 54 | Alati | Esineb 1 haiguses |
| FOXJ1forkhead box J1 | Alati | Esineb 2 haiguses |
| ODAD4outer dynein arm docking complex subunit 4 | Alati | Esineb 2 haiguses |
| PTCRApre T cell antigen receptor alpha | Alati | Esineb 1 haiguses |
| CFTRCF transmembrane conductance regulator | Väga sageli (80–99%) | Esineb 1 haiguses |
| ODAD1outer dynein arm docking complex subunit 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SCNN1Asodium channel epithelial 1 subunit alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| SCNN1Bsodium channel epithelial 1 subunit beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Väga sageli (80–99%) | Esineb 1 haiguses |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | Sageli (30–79%) | Esineb 1 haiguses |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | Sageli (30–79%) | Esineb 1 haiguses |
| CCNOcyclin O | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP221cilia and flagella associated protein 221 | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP298cilia and flagella associated protein 298 | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP74cilia and flagella associated protein 74 | Sageli (30–79%) | Esineb 1 haiguses |
| CLXNcalaxin | Sageli (30–79%) | Esineb 1 haiguses |
| DAW1dynein assembly factor with WD repeats 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF1dynein axonemal assembly factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF11dynein axonemal assembly factor 11 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF19dynein axonemal assembly factor 19 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF2dynein axonemal assembly factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF3dynein axonemal assembly factor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF4dynein axonemal assembly factor 4 | Sageli (30–79%) | Esineb 2 haiguses |
| DNAAF5dynein axonemal assembly factor 5 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAAF6dynein axonemal assembly factor 6 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAH1dynein axonemal heavy chain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAH11dynein axonemal heavy chain 11 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAH5dynein axonemal heavy chain 5 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAH7dynein axonemal heavy chain 7 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAH9dynein axonemal heavy chain 9 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAI1dynein axonemal intermediate chain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAI2dynein axonemal intermediate chain 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAJB13DnaJ heat shock protein family (Hsp40) member B13 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAL1dynein axonemal light chain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DRC1dynein regulatory complex subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DRC2dynein regulatory complex subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DRC4dynein regulatory complex subunit 4 | Sageli (30–79%) | Esineb 1 haiguses |
| GAS2L2growth arrest specific 2 like 2 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 33 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| HYDINHYDIN axonemal central pair apparatus protein | Sageli (30–79%) | Esineb 1 haiguses |
| LRRC56leucine rich repeat containing 56 | Sageli (30–79%) | Esineb 1 haiguses |
| MCIDASmulticiliate differentiation and DNA synthesis associated cell cycle protein | Sageli (30–79%) | Esineb 1 haiguses |
| NEK10NIMA related kinase 10 | Sageli (30–79%) | Esineb 1 haiguses |
| NME5NME/NM23 family member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| NME8NME/NM23 family member 8 | Sageli (30–79%) | Esineb 1 haiguses |
| ODAD2outer dynein arm docking complex subunit 2 | Sageli (30–79%) | Esineb 2 haiguses |
| ODAD3outer dynein arm docking complex subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| OFD1OFD1 centriole and centriolar satellite protein | Sageli (30–79%) | Esineb 1 haiguses |
| RPGRretinitis pigmentosa GTPase regulator | Sageli (30–79%) | Esineb 1 haiguses |
| RSPH1radial spoke head component 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RSPH3radial spoke head 3 | Sageli (30–79%) | Esineb 1 haiguses |
| RSPH4Aradial spoke head component 4A | Sageli (30–79%) | Esineb 1 haiguses |
| RSPH9radial spoke head component 9 | Sageli (30–79%) | Esineb 1 haiguses |
| SPAG1sperm associated antigen 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SPEF2sperm flagellar and cilia associated 2 | Sageli (30–79%) | Esineb 1 haiguses |
| STK36serine/threonine kinase 36 | Sageli (30–79%) | Esineb 1 haiguses |
| TTC12tetratricopeptide repeat domain 12 | Sageli (30–79%) | Esineb 1 haiguses |
| ZMYND10zinc finger MYND-type containing 10 | Sageli (30–79%) | Esineb 1 haiguses |
| ARL2BPARF like GTPase 2 binding protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCORBCL6 corepressor | Mõnikord (5–29%) | Esineb 1 haiguses |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NABP1nucleic acid binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPM1nucleophosmin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NUMA1nuclear mitotic apparatus protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PMLPML nuclear body scaffold | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| RARAretinoic acid receptor alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| STAT3signal transducer and activator of transcription 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STAT5Bsignal transducer and activator of transcription 5B | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBL1XR1TBL1X/Y related 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZBTB16zinc finger and BTB domain containing 16 | Mõnikord (5–29%) | 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