Tunnus
Postural tremor
A type of tremors that is triggered by holding a limb in a fixed position.
Kokkuvõte
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Postural tremor, and the rest of your genome, with one test.
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Telli oma Genome Test67 geeni on seotud tunnusega Postural tremor
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Postural tremor. 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 |
|---|---|---|
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Alati | Esineb 2 haiguses |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alati | Esineb 2 haiguses |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Alati | Esineb 1 haiguses |
| RILPL1Rab interacting lysosomal protein like 1 | Alati | Esineb 1 haiguses |
| TENM4teneurin transmembrane protein 4 | Alati | Esineb 1 haiguses |
| VAPBVAMP associated protein B and C | Alati | Esineb 1 haiguses |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| MYBPC1myosin binding protein C1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TPP1tripeptidyl peptidase 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Sageli (30–79%) | Esineb 2 haiguses |
| ATXN2ataxin 2 | Sageli (30–79%) | Esineb 2 haiguses |
| COL6A3collagen type VI alpha 3 chain | Sageli (30–79%) | Esineb 1 haiguses |
| COQ2coenzyme Q2, polyprenyltransferase | Sageli (30–79%) | Esineb 2 haiguses |
| COQ4coenzyme Q4 | Sageli (30–79%) | Esineb 1 haiguses |
| GALTgalactose-1-phosphate uridylyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| GCH1GTP cyclohydrolase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| IMPDH2inosine monophosphate dehydrogenase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MPZmyelin protein zero | Sageli (30–79%) | Esineb 1 haiguses |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Sageli (30–79%) | Esineb 2 haiguses |
| OPA3outer mitochondrial membrane lipid metabolism regulator OPA3 | Sageli (30–79%) | Esineb 1 haiguses |
| PARK7Parkinsonism associated deglycase | Sageli (30–79%) | Esineb 1 haiguses |
| PMP22peripheral myelin protein 22 | Sageli (30–79%) | Esineb 1 haiguses |
| POLR3ARNA polymerase III subunit A | Sageli (30–79%) | Esineb 2 haiguses |
| PRDX3peroxiredoxin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| PRKNparkin RBR E3 ubiquitin protein ligase | Sageli (30–79%) | Esineb 1 haiguses |
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | Sageli (30–79%) | Esineb 2 haiguses |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC9A6solute carrier family 9 member A6 | Sageli (30–79%) | Esineb 1 haiguses |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Sageli (30–79%) | Esineb 1 haiguses |
| THtyrosine hydroxylase | Sageli (30–79%) | Esineb 1 haiguses |
| TMEM240transmembrane protein 240 | Sageli (30–79%) | Esineb 1 haiguses |
| TSPOAP1TSPO associated protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| UCHL1ubiquitin C-terminal hydrolase L1 | Sageli (30–79%) | Esineb 1 haiguses |
| ATXN1ataxin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FGF14fibroblast growth factor 14 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MFN2mitofusin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Mõnikord (5–29%) | Esineb 2 haiguses |
Näita veel 27 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-CYBmitochondrially encoded cytochrome b | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-ND4Lmitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4L | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Mõnikord (5–29%) | Esineb 2 haiguses |
| NDRG1N-myc downstream regulated 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NIPA1NIPA magnesium transporter 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPTX1neuronal pentraxin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDGFBplatelet derived growth factor subunit B | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIK3R5phosphoinositide-3-kinase regulatory subunit 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | Mõnikord (5–29%) | Esineb 1 haiguses |
| REEP2receptor accessory protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SETXsenataxin | Mõnikord (5–29%) | Esineb 1 haiguses |
| STUB1STIP1 homology and U-box containing protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP13A2ATPase cation transporting 13A2 | Harva (1–4%) | Esineb 1 haiguses |
| DRD3dopamine receptor D3 | Pole registreeritud | Esineb 1 haiguses |
| FMR1fragile X messenger ribonucleoprotein 1 | Pole registreeritud | Esineb 1 haiguses |
| FUSFUS RNA binding protein | Pole registreeritud | Esineb 1 haiguses |
| KCND3potassium voltage-gated channel subfamily D member 3 | Pole registreeritud | Esineb 1 haiguses |
| NOTCH2NLCnotch 2 N-terminal like C | Pole registreeritud | Esineb 1 haiguses |
| POLR3BRNA polymerase III subunit B | Pole registreeritud | Esineb 1 haiguses |
| SCARB2scavenger receptor class B 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.
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