Tunnus
Dizziness
Kliiniline nimetus: Vertigo
An abnormal sensation of spinning while the body is actually stationary.
Kokkuvõte
- Teised nimetused
- Dizzy spell
- Kehasüsteem
- Abnormality of the ear
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Dizziness, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test140 geeni on seotud tunnusega Dizziness
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Dizziness. 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 |
|---|---|---|
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Alati | Esineb 1 haiguses |
| EMDemerin | Alati | Esineb 1 haiguses |
| FDXRferredoxin reductase | Alati | Esineb 1 haiguses |
| GCGRglucagon receptor | Alati | Esineb 1 haiguses |
| LAMB1laminin subunit beta 1 | Alati | Esineb 1 haiguses |
| MAU2MAU2 sister chromatid cohesion factor | Alati | Esineb 1 haiguses |
| NOTCH3notch receptor 3 | Alati | Esineb 1 haiguses |
| RFC4replication factor C subunit 4 | Alati | Esineb 1 haiguses |
| RRP12ribosomal RNA processing 12 homolog | Alati | Esineb 2 haiguses |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Alati | Esineb 2 haiguses |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Alati | Esineb 1 haiguses |
| ADA2adenosine deaminase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Väga sageli (80–99%) | Esineb 6 haiguses |
| EPORerythropoietin receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| JAK2Janus kinase 2 | Väga sageli (80–99%) | Esineb 4 haiguses |
| JUPjunction plakoglobin | Väga sageli (80–99%) | Esineb 1 haiguses |
| NAGAalpha-N-acetylgalactosaminidase | Väga sageli (80–99%) | Esineb 3 haiguses |
| SLC1A3solute carrier family 1 member 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ABCC9ATP binding cassette subfamily C member 9 | Sageli (30–79%) | Esineb 1 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Sageli (30–79%) | Esineb 2 haiguses |
| BCORBCL6 corepressor | Sageli (30–79%) | Esineb 1 haiguses |
| CACNB4calcium voltage-gated channel auxiliary subunit beta 4 | Sageli (30–79%) | Esineb 2 haiguses |
| CALRcalreticulin | Sageli (30–79%) | Esineb 1 haiguses |
| CCND1cyclin D1 | Sageli (30–79%) | Esineb 2 haiguses |
| CMPK2cytidine/uridine monophosphate kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DKK1dickkopf Wnt signaling pathway inhibitor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Sageli (30–79%) | Esineb 1 haiguses |
| GATA2GATA binding protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| GATA4GATA binding protein 4 | Sageli (30–79%) | Esineb 1 haiguses |
| GATA5GATA binding protein 5 | Sageli (30–79%) | Esineb 1 haiguses |
| GATA6GATA binding protein 6 | Sageli (30–79%) | Esineb 1 haiguses |
| GJA5gap junction protein alpha 5 | Sageli (30–79%) | Esineb 1 haiguses |
| GYG1glycogenin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| JAM2junctional adhesion molecule 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| KCNA5potassium voltage-gated channel subfamily A member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 100 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| KCNJ3potassium inwardly rectifying channel subfamily J member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| LRP4LDL receptor related protein 4 | Sageli (30–79%) | Esineb 1 haiguses |
| MPLMPL proto-oncogene, thrombopoietin receptor | Sageli (30–79%) | Esineb 2 haiguses |
| MYD88MYD88 innate immune signal transduction adaptor | Sageli (30–79%) | Esineb 1 haiguses |
| MYL4myosin light chain 4 | Sageli (30–79%) | Esineb 1 haiguses |
| MYORGmyogenesis regulating glycosidase | Sageli (30–79%) | Esineb 1 haiguses |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| NABP1nucleic acid binding protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NKX2-5NK2 homeobox 5 | Sageli (30–79%) | Esineb 2 haiguses |
| NKX2-6NK2 homeobox 6 | Sageli (30–79%) | Esineb 1 haiguses |
| NPM1nucleophosmin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NPPAnatriuretic peptide A | Sageli (30–79%) | Esineb 2 haiguses |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NUMA1nuclear mitotic apparatus protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NUP155nucleoporin 155 | Sageli (30–79%) | Esineb 1 haiguses |
| PDGFBplatelet derived growth factor subunit B | Sageli (30–79%) | Esineb 2 haiguses |
| PDGFRBplatelet derived growth factor receptor beta | Sageli (30–79%) | Esineb 1 haiguses |
| PITX2paired like homeodomain 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PMLPML nuclear body scaffold | Sageli (30–79%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| PRRT2proline rich transmembrane protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RARAretinoic acid receptor alpha | Sageli (30–79%) | Esineb 1 haiguses |
| RYR1ryanodine receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN4Bsodium voltage-gated channel beta subunit 4 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Sageli (30–79%) | Esineb 3 haiguses |
| SH2B3SH2B adaptor protein 3 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC20A2solute carrier family 20 member 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SRPK3SRSF protein kinase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| STAT3signal transducer and activator of transcription 3 | Sageli (30–79%) | Esineb 1 haiguses |
| STAT5Bsignal transducer and activator of transcription 5B | Sageli (30–79%) | Esineb 1 haiguses |
| SUFUSUFU negative regulator of hedgehog signaling | Sageli (30–79%) | Esineb 1 haiguses |
| TBL1XR1TBL1X/Y related 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TET2tet methylcytosine dioxygenase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TP53tumor protein p53 | Sageli (30–79%) | Esineb 1 haiguses |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Sageli (30–79%) | Esineb 1 haiguses |
| TTNtitin | Sageli (30–79%) | Esineb 1 haiguses |
| VHLvon Hippel-Lindau tumor suppressor | Sageli (30–79%) | Esineb 2 haiguses |
| VSX1visual system homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ZBTB16zinc finger and BTB domain containing 16 | Sageli (30–79%) | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Mõnikord (5–29%) | Esineb 1 haiguses |
| C4Acomplement C4A (Chido/Rodgers blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCR1C-C motif chemokine receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDH23cadherin related 23 | Mõnikord (5–29%) | Esineb 2 haiguses |
| CHD2chromodomain helicase DNA binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CNNM2cyclin and CBS domain divalent metal cation transport mediator 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CUX2cut like homeobox 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DBHdopamine beta-hydroxylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNM1dynamin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FASFas cell surface death receptor | Mõnikord (5–29%) | Esineb 2 haiguses |
| FGF14fibroblast growth factor 14 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| FOXI1forkhead box I1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GABRB3gamma-aminobutyric acid type A receptor subunit beta3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GCDHglutaryl-CoA dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Mõnikord (5–29%) | Esineb 3 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| IFNGR1interferon gamma receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL10interleukin 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL12Ainterleukin 12A | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL12A-AS1IL12A antisense RNA 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL12Binterleukin 12B | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL23Rinterleukin 23 receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KLRC4killer cell lectin like receptor C4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAPK10mitogen-activated protein kinase 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MED12mediator complex subunit 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEFVMEFV innate immunity regulator, pyrin | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEN1menin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MLXMAX dimerization protein MLX | Mõnikord (5–29%) | Esineb 1 haiguses |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Mõnikord (5–29%) | Esineb 1 haiguses |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SLC26A4solute carrier family 26 member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STAT4signal transducer and activator of transcription 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| THPOthrombopoietin | Mõnikord (5–29%) | Esineb 1 haiguses |
| TLR4toll like receptor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNFRSF1ATNF receptor superfamily member 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBAC2UBA domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Harva (1–4%) | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Harva (1–4%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Harva (1–4%) | Esineb 1 haiguses |
| NOP56NOP56 ribonucleoprotein | Harva (1–4%) | Esineb 1 haiguses |
| SLC12A3solute carrier family 12 member 3 | Harva (1–4%) | Esineb 2 haiguses |
| CALM1calmodulin 1 | Pole registreeritud | Esineb 1 haiguses |
| COCHcochlin | Pole registreeritud | Esineb 1 haiguses |
| MVKmevalonate kinase | Pole registreeritud | Esineb 1 haiguses |
| MYL2myosin light chain 2 | Pole registreeritud | Esineb 1 haiguses |
| MYO7Amyosin VIIA | Pole registreeritud | Esineb 2 haiguses |
| TPK1thiamin pyrophosphokinase 1 | 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.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast