Tunnus
Confusion
Lack of clarity and coherence of thought, perception, understanding, or action.
Kokkuvõte
- Teised nimetused
- Disorientation, Easily confused, Mental disorientation
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Confusion, and the rest of your genome, with one test.
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Telli oma Genome Test72 geeni on seotud tunnusega Confusion
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Confusion. 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 |
|---|---|---|
| LAMB1laminin subunit beta 1 | Alati | Esineb 1 haiguses |
| TLR3toll like receptor 3 | Alati | Esineb 1 haiguses |
| UQCRHubiquinol-cytochrome c reductase hinge protein | Alati | Esineb 1 haiguses |
| APPamyloid beta precursor protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| HADHhydroxyacyl-CoA dehydrogenase | Väga sageli (80–99%) | Esineb 1 haiguses |
| PSEN1presenilin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PSEN2presenilin 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLC22A5solute carrier family 22 member 5 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SORL1sortilin related receptor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TOMM40translocase of outer mitochondrial membrane 40 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TRANK1tetratricopeptide repeat and ankyrin repeat containing 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TREM2triggering receptor expressed on myeloid cells 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| APOEapolipoprotein E | Sageli (30–79%) | Esineb 1 haiguses |
| ATP13A2ATPase cation transporting 13A2 | Sageli (30–79%) | Esineb 1 haiguses |
| C4Acomplement C4A (Chido/Rodgers blood group) | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Sageli (30–79%) | Esineb 2 haiguses |
| CCR1C-C motif chemokine receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EPM2AEPM2A glucan phosphatase, laforin | Sageli (30–79%) | Esineb 1 haiguses |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC5ERCC excision repair 5, endonuclease | Sageli (30–79%) | Esineb 1 haiguses |
| FASFas cell surface death receptor | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Sageli (30–79%) | Esineb 1 haiguses |
| IFNGR1interferon gamma receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| IL10interleukin 10 | Sageli (30–79%) | Esineb 1 haiguses |
| IL12Ainterleukin 12A | Sageli (30–79%) | Esineb 1 haiguses |
| IL12A-AS1IL12A antisense RNA 1 | Sageli (30–79%) | Esineb 1 haiguses |
| IL23Rinterleukin 23 receptor | Sageli (30–79%) | Esineb 1 haiguses |
| KLRC4killer cell lectin like receptor C4 | Sageli (30–79%) | Esineb 1 haiguses |
| MEFVMEFV innate immunity regulator, pyrin | Sageli (30–79%) | Esineb 1 haiguses |
| NAXENAD(P)HX epimerase | Sageli (30–79%) | Esineb 1 haiguses |
| NHLRC1NHL repeat containing E3 ubiquitin protein ligase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| POLR3ARNA polymerase III subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| PRNPprion protein (Kanno blood group) | Sageli (30–79%) | Esineb 2 haiguses |
| PRRT2proline rich transmembrane protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC19A3solute carrier family 19 member 3 | Sageli (30–79%) | Esineb 2 haiguses |
Näita veel 32 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SLC25A13solute carrier family 25 member 13 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC25A15solute carrier family 25 member 15 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC2A1solute carrier family 2 member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| STAT4signal transducer and activator of transcription 4 | Sageli (30–79%) | Esineb 1 haiguses |
| TLR4toll like receptor 4 | Sageli (30–79%) | Esineb 1 haiguses |
| TTRtransthyretin | Sageli (30–79%) | Esineb 1 haiguses |
| UBAC2UBA domain containing 2 | Sageli (30–79%) | Esineb 1 haiguses |
| VPS13Cvacuolar protein sorting 13 homolog C | Sageli (30–79%) | Esineb 1 haiguses |
| ABCD1ATP binding cassette subfamily D member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALADaminolevulinate dehydratase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTSFcathepsin F | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNASGNAS complex locus | Mõnikord (5–29%) | Esineb 2 haiguses |
| HMBShydroxymethylbilane synthase | Mõnikord (5–29%) | Esineb 1 haiguses |
| IVDisovaleryl-CoA dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAN2B1mannosidase alpha class 2B member 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MEN1menin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAGSN-acetylglutamate synthase | Mõnikord (5–29%) | Esineb 2 haiguses |
| NOTCH3notch receptor 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRDM8PR/SET domain 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RYR1ryanodine receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ADAMTS13ADAM metallopeptidase with thrombospondin type 1 motif 13 | Pole registreeritud | Esineb 1 haiguses |
| CHRNA2cholinergic receptor nicotinic alpha 2 subunit | Pole registreeritud | Esineb 1 haiguses |
| CPOXcoproporphyrinogen oxidase | Pole registreeritud | Esineb 1 haiguses |
| CUBNcubilin | Pole registreeritud | Esineb 1 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Pole registreeritud | Esineb 1 haiguses |
| MMACHCmetabolism of cobalamin associated C | Pole registreeritud | Esineb 1 haiguses |
| PRDX1peroxiredoxin 1 | Pole registreeritud | Esineb 1 haiguses |
| TBK1TANK binding kinase 1 | Pole registreeritud | Esineb 1 haiguses |
| TBPTATA-box binding protein | 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