Træk
Slow movements
Klinisk navn: Bradykinesia
Bradykinesia literally means slow movement, and is used clinically to denote a slowness in the execution of movement (in contrast to hypokinesia, which is used to refer to slowness in the initiation of movement).
Resumé
- Også kaldet
- Slowness of movements
- Kropssystem
- Abnormality of the nervous system
ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
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Bestil min Genome Test130 gener knyttet til Slow movements
Ændringer i disse gener forårsager sjældne tilstande, hvor Slow movements ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| AHDC1AT-hook DNA binding motif containing 1 | Altid | I 1 tilstand |
| ATP13A2ATPase cation transporting 13A2 | Altid | I 4 tilstande |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Altid | I 3 tilstande |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Altid | I 3 tilstande |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Altid | I 3 tilstande |
| EIF2AK1eukaryotic translation initiation factor 2 alpha kinase 1 | Altid | I 1 tilstand |
| EPG5ectopic P-granules 5 autophagy tethering factor | Altid | I 1 tilstand |
| HTThuntingtin | Altid | I 4 tilstande |
| LRRC7leucine rich repeat containing 7 | Altid | I 1 tilstand |
| MAPTmicrotubule associated protein tau | Altid | I 6 tilstande |
| MECP2methyl-CpG binding protein 2 | Altid | I 2 tilstande |
| MYORGmyogenesis regulating glycosidase | Altid | I 3 tilstande |
| PARK7Parkinsonism associated deglycase | Altid | I 2 tilstande |
| PDE8Bphosphodiesterase 8B | Altid | I 2 tilstande |
| PET117PET117 cytochrome c oxidase chaperone | Altid | I 1 tilstand |
| PLA2G6phospholipase A2 group VI | Altid | I 3 tilstande |
| POLGDNA polymerase gamma, catalytic subunit | Altid | I 4 tilstande |
| PRKNparkin RBR E3 ubiquitin protein ligase | Altid | I 2 tilstande |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | Altid | I 1 tilstand |
| RAB32RAB32, member RAS oncogene family | Altid | I 1 tilstand |
| RAB39BRAB39B, member RAS oncogene family | Altid | I 1 tilstand |
| SNCAsynuclein alpha | Altid | I 4 tilstande |
| SYNJ1synaptojanin 1 | Altid | I 3 tilstande |
| UQCRC1ubiquinol-cytochrome c reductase core protein 1 | Altid | I 1 tilstand |
| CHCHD2coiled-coil-helix-coiled-coil-helix domain containing 2 | Meget ofte (80–99 %) | I 1 tilstand |
| NIT1nitrilase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| PODXLpodocalyxin like | Meget ofte (80–99 %) | I 2 tilstande |
| SLC6A3solute carrier family 6 member 3 | Meget ofte (80–99 %) | I 2 tilstande |
| ACTA1actin alpha 1, skeletal muscle | Ofte (30–79 %) | I 1 tilstand |
| ATCAYATCAY kinesin light chain interacting caytaxin | Ofte (30–79 %) | I 1 tilstand |
| ATXN1ataxin 1 | Ofte (30–79 %) | I 1 tilstand |
| ATXN10ataxin 10 | Ofte (30–79 %) | I 1 tilstand |
| ATXN8ataxin 8 | Ofte (30–79 %) | I 1 tilstand |
| ATXN8OSATXN8 opposite strand lncRNA | Ofte (30–79 %) | I 2 tilstande |
| CMPK2cytidine/uridine monophosphate kinase 2 | Ofte (30–79 %) | I 1 tilstand |
| COQ2coenzyme Q2, polyprenyltransferase | Ofte (30–79 %) | I 3 tilstande |
| EIF2AK2eukaryotic translation initiation factor 2 alpha kinase 2 | Ofte (30–79 %) | I 1 tilstand |
| FBXO7F-box protein 7 | Ofte (30–79 %) | I 2 tilstande |
| FGF13fibroblast growth factor 13 | Ofte (30–79 %) | I 2 tilstande |
| FTLferritin light chain | Ofte (30–79 %) | I 2 tilstande |
Vis 90 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Ofte (30–79 %) | I 1 tilstand |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Ofte (30–79 %) | I 2 tilstande |
| GCH1GTP cyclohydrolase 1 | Ofte (30–79 %) | I 2 tilstande |
| JAM2junctional adhesion molecule 2 | Ofte (30–79 %) | I 3 tilstande |
| KBTBD13kelch repeat and BTB domain containing 13 | Ofte (30–79 %) | I 1 tilstand |
| KLHL41kelch like family member 41 | Ofte (30–79 %) | I 1 tilstand |
| MYPNmyopalladin | Ofte (30–79 %) | I 1 tilstand |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Ofte (30–79 %) | I 2 tilstande |
| NEBnebulin | Ofte (30–79 %) | I 1 tilstand |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Ofte (30–79 %) | I 3 tilstande |
| PCDH19protocadherin 19 | Ofte (30–79 %) | I 1 tilstand |
| PDGFBplatelet derived growth factor subunit B | Ofte (30–79 %) | I 2 tilstande |
| PDGFRBplatelet derived growth factor receptor beta | Ofte (30–79 %) | I 2 tilstande |
| POLG2DNA polymerase gamma 2, accessory subunit | Ofte (30–79 %) | I 1 tilstand |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Ofte (30–79 %) | I 1 tilstand |
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | Ofte (30–79 %) | I 2 tilstande |
| PRNPprion protein (Kanno blood group) | Ofte (30–79 %) | I 3 tilstande |
| PTPAprotein phosphatase 2 phosphatase activator | Ofte (30–79 %) | I 1 tilstand |
| RAB3ARAB3A, member RAS oncogene family | Ofte (30–79 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Ofte (30–79 %) | I 1 tilstand |
| RRP12ribosomal RNA processing 12 homolog | Ofte (30–79 %) | I 2 tilstande |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Ofte (30–79 %) | I 2 tilstande |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Ofte (30–79 %) | I 2 tilstande |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Ofte (30–79 %) | I 2 tilstande |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Ofte (30–79 %) | I 2 tilstande |
| SLC20A2solute carrier family 20 member 2 | Ofte (30–79 %) | I 2 tilstande |
| SLC25A4solute carrier family 25 member 4 | Ofte (30–79 %) | I 1 tilstand |
| SLC2A3solute carrier family 2 member 3 | Ofte (30–79 %) | I 1 tilstand |
| SLC30A10solute carrier family 30 member 10 | Ofte (30–79 %) | I 2 tilstande |
| SLC39A14solute carrier family 39 member 14 | Ofte (30–79 %) | I 2 tilstande |
| SLC9A6solute carrier family 9 member A6 | Ofte (30–79 %) | I 1 tilstand |
| SPRsepiapterin reductase | Ofte (30–79 %) | I 1 tilstand |
| TAF1TATA-box binding protein associated factor 1 | Ofte (30–79 %) | I 1 tilstand |
| THtyrosine hydroxylase | Ofte (30–79 %) | I 1 tilstand |
| TPM2tropomyosin 2 | Ofte (30–79 %) | I 1 tilstand |
| TPM3tropomyosin 3 | Ofte (30–79 %) | I 1 tilstand |
| TSPOAP1TSPO associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Ofte (30–79 %) | I 1 tilstand |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Ofte (30–79 %) | I 1 tilstand |
| WDR45WD repeat domain 45 | Ofte (30–79 %) | I 2 tilstande |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Ofte (30–79 %) | I 2 tilstande |
| ATP5MKATP synthase membrane subunit k | Nogle gange (5–29 %) | I 1 tilstand |
| CLTCclathrin heavy chain | Nogle gange (5–29 %) | I 1 tilstand |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Nogle gange (5–29 %) | I 1 tilstand |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Nogle gange (5–29 %) | I 2 tilstande |
| FARS2phenylalanyl-tRNA synthetase 2, mitochondrial | Nogle gange (5–29 %) | I 1 tilstand |
| FMR1fragile X messenger ribonucleoprotein 1 | Nogle gange (5–29 %) | I 2 tilstande |
| GBA1glucosylceramidase beta 1 | Nogle gange (5–29 %) | I 2 tilstande |
| GIGYF2GRB10 interacting GYF protein 2 | Nogle gange (5–29 %) | I 2 tilstande |
| HTRA2HtrA serine peptidase 2 | Nogle gange (5–29 %) | I 2 tilstande |
| IMPDH2inosine monophosphate dehydrogenase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| LRRK2leucine rich repeat kinase 2 | Nogle gange (5–29 %) | I 3 tilstande |
| PIDD1p53-induced death domain protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PINK1PTEN induced kinase 1 | Nogle gange (5–29 %) | I 2 tilstande |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | Nogle gange (5–29 %) | I 1 tilstand |
| PRDX3peroxiredoxin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| PTS6-pyruvoyltetrahydropterin synthase | Nogle gange (5–29 %) | I 2 tilstande |
| RRM1ribonucleotide reductase catalytic subunit M1 | Nogle gange (5–29 %) | I 1 tilstand |
| TACO1translational activator of cytochrome c oxidase I | Nogle gange (5–29 %) | I 1 tilstand |
| TK2thymidine kinase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TOP3ADNA topoisomerase III alpha | Nogle gange (5–29 %) | I 1 tilstand |
| TTC19tetratricopeptide repeat domain 19 | Nogle gange (5–29 %) | I 1 tilstand |
| UCHL1ubiquitin C-terminal hydrolase L1 | Nogle gange (5–29 %) | I 2 tilstande |
| VPS13Avacuolar protein sorting 13 homolog A | Nogle gange (5–29 %) | I 1 tilstand |
| VPS13Cvacuolar protein sorting 13 homolog C | Nogle gange (5–29 %) | I 1 tilstand |
| VPS35VPS35 retromer complex component | Nogle gange (5–29 %) | I 2 tilstande |
| ADGRV1adhesion G protein-coupled receptor V1 | Sjældent (1–4%) | I 1 tilstand |
| ATL1atlastin GTPase 1 | Sjældent (1–4%) | I 1 tilstand |
| CPA6carboxypeptidase A6 | Sjældent (1–4%) | I 1 tilstand |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Sjældent (1–4%) | I 1 tilstand |
| HCN1hyperpolarization activated cyclic nucleotide gated potassium channel 1 | Sjældent (1–4%) | I 1 tilstand |
| KCNC3potassium voltage-gated channel subfamily C member 3 | Sjældent (1–4%) | I 1 tilstand |
| PRRT2proline rich transmembrane protein 2 | Sjældent (1–4%) | I 1 tilstand |
| SLC32A1solute carrier family 32 member 1 | Sjældent (1–4%) | I 1 tilstand |
| STX1Bsyntaxin 1B | Sjældent (1–4%) | I 1 tilstand |
| ADH1Calcohol dehydrogenase 1C (class I), gamma polypeptide | Ikke registreret | I 1 tilstand |
| ATXN2ataxin 2 | Ikke registreret | I 2 tilstande |
| ATXN3ataxin 3 | Ikke registreret | I 2 tilstande |
| COASYCoenzyme A synthase | Ikke registreret | I 1 tilstand |
| CSF1Rcolony stimulating factor 1 receptor | Ikke registreret | I 1 tilstand |
| DCTN1dynactin subunit 1 | Ikke registreret | I 1 tilstand |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Ikke registreret | I 1 tilstand |
| DNAJC12DnaJ heat shock protein family (Hsp40) member C12 | Ikke registreret | I 1 tilstand |
| EARS2glutamyl-tRNA synthetase 2, mitochondrial | Ikke registreret | I 1 tilstand |
| JPH3junctophilin 3 | Ikke registreret | I 1 tilstand |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | Ikke registreret | I 1 tilstand |
| PANK2pantothenate kinase 2 | Ikke registreret | I 1 tilstand |
| SNCAIPsynuclein alpha interacting protein | Ikke registreret | I 1 tilstand |
| TBPTATA-box binding protein | Ikke registreret | I 2 tilstande |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.16-c6eea6bf.
Én test. Svar for hele livet.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger