Tunnus
Clonus
A series of rhythmic and involuntary muscle contractions (at a frequency of about 5 to 7 Hz) that occur in response to an abruptly applied and sustained stretch.
Kokkuvõte
- Teised nimetused
- Involuntary rhythmic muscular contractions and relaxations
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Clonus, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test98 geeni on seotud tunnusega Clonus
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Clonus. 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 |
|---|---|---|
| ABCB7ATP binding cassette subfamily B member 7 | Alati | Esineb 1 haiguses |
| CAMLGcalcium modulating ligand | Alati | Esineb 1 haiguses |
| CCT5chaperonin containing TCP1 subunit 5 | Alati | Esineb 2 haiguses |
| DNM1dynamin 1 | Alati | Esineb 1 haiguses |
| DNM1Ldynamin 1L | Alati | Esineb 1 haiguses |
| GOLGA2golgin A2 | Alati | Esineb 1 haiguses |
| GTF3C3general transcription factor IIIC subunit 3 | Alati | Esineb 1 haiguses |
| KLC4kinesin light chain 4 | Alati | Esineb 1 haiguses |
| MED17mediator complex subunit 17 | Alati | Esineb 1 haiguses |
| MICU1mitochondrial calcium uptake 1 | Alati | Esineb 1 haiguses |
| MSL2MSL complex subunit 2 | Alati | Esineb 1 haiguses |
| MYL2myosin light chain 2 | Alati | Esineb 1 haiguses |
| NADK2NAD kinase 2, mitochondrial | Alati | Esineb 1 haiguses |
| NFU1NFU1 iron-sulfur cluster scaffold | Alati | Esineb 1 haiguses |
| NSD1nuclear receptor binding SET domain protein 1 | Alati | Esineb 1 haiguses |
| PGBD5piggyBac transposable element derived 5 | Alati | Esineb 1 haiguses |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Alati | Esineb 1 haiguses |
| SEL1LSEL1L adaptor subunit of SYVN1 ubiquitin ligase | Alati | Esineb 1 haiguses |
| SLC25A21solute carrier family 25 member 21 | Alati | Esineb 1 haiguses |
| TANGO2transport and golgi organization 2 homolog | Alati | Esineb 2 haiguses |
| TSEN2tRNA splicing endonuclease subunit 2 | Alati | Esineb 1 haiguses |
| WDR83OSWD repeat domain 83 opposite strand | Alati | Esineb 1 haiguses |
| TIMM50translocase of inner mitochondrial membrane 50 | Väga sageli (80–99%) | Esineb 2 haiguses |
| VPS37AVPS37A subunit of ESCRT-I | Väga sageli (80–99%) | Esineb 2 haiguses |
| ALS2alsin Rho guanine nucleotide exchange factor ALS2 | Sageli (30–79%) | Esineb 2 haiguses |
| AMPD2adenosine monophosphate deaminase 2 | Sageli (30–79%) | Esineb 2 haiguses |
| ASNSasparagine synthetase (glutamine-hydrolyzing) | Sageli (30–79%) | Esineb 1 haiguses |
| DTYMKdeoxythymidylate kinase | Sageli (30–79%) | Esineb 1 haiguses |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EMILIN1elastin microfibril interfacer 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EXTL3exostosin like glycosyltransferase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNQ3potassium voltage-gated channel subfamily Q member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| KIF1Ckinesin family member 1C | Sageli (30–79%) | Esineb 1 haiguses |
| NOTCH3notch receptor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Sageli (30–79%) | Esineb 1 haiguses |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PRUNE1prune exopolyphosphatase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| RTN2reticulon 2 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 58 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| RUSC2RUN and SH3 domain containing 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC25A15solute carrier family 25 member 15 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC33A1solute carrier family 33 member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC44A1solute carrier family 44 member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| UBAP1ubiquitin associated protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| USP8ubiquitin specific peptidase 8 | Sageli (30–79%) | Esineb 1 haiguses |
| ATP13A2ATPase cation transporting 13A2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRELD1CRELD disulfide isomerase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EBF3EBF transcription factor 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERLIN1ER lipid raft associated 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| FKRPfukutin related protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| FUSFUS RNA binding protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| GMPPBGDP-mannose pyrophosphorylase B | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HTRA2HtrA serine peptidase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HTThuntingtin | Mõnikord (5–29%) | Esineb 1 haiguses |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Mõnikord (5–29%) | Esineb 1 haiguses |
| KDM1Alysine demethylase 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| KPNA3karyopherin subunit alpha 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMNB1lamin B1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDPnorrin cystine knot growth factor NDP | Mõnikord (5–29%) | Esineb 1 haiguses |
| PCpyruvate carboxylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PET100PET100 cytochrome c oxidase chaperone | Mõnikord (5–29%) | Esineb 1 haiguses |
| PEX16peroxisomal biogenesis factor 16 | Mõnikord (5–29%) | Esineb 1 haiguses |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Mõnikord (5–29%) | Esineb 1 haiguses |
| POMKprotein O-mannose kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| POMT1protein O-mannosyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| POMT2protein O-mannosyltransferase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTS6-pyruvoyltetrahydropterin synthase | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNASEH1ribonuclease H1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU4-2RNA, U4 small nuclear 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SETXsenataxin | Mõnikord (5–29%) | Esineb 1 haiguses |
| SIGMAR1sigma receptor chaperone 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC1A4solute carrier family 1 member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC2A3solute carrier family 2 member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SORDsorbitol dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TARDBPTAR DNA binding protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRMT2BtRNA methyltransferase 2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBQLN2ubiquilin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| WASHC5WASH complex subunit 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Harva (1–4%) | Esineb 1 haiguses |
| BRAT1BRCA1 associated ATM activator 1 | Pole registreeritud | Esineb 1 haiguses |
| CAV1caveolin 1 | Pole registreeritud | Esineb 1 haiguses |
| HIKESHIheat shock protein nuclear import factor hikeshi | Pole registreeritud | Esineb 1 haiguses |
| KCNT1potassium sodium-activated channel subfamily T member 1 | Pole registreeritud | Esineb 1 haiguses |
| NIPA1NIPA magnesium transporter 1 | Pole registreeritud | Esineb 1 haiguses |
| PIGPphosphatidylinositol glycan anchor biosynthesis class P | Pole registreeritud | Esineb 1 haiguses |
| SEPSECSSep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase | Pole registreeritud | Esineb 1 haiguses |
| SLC16A2solute carrier family 16 member 2 | Pole registreeritud | Esineb 1 haiguses |
| SLC6A9solute carrier family 6 member 9 | Pole registreeritud | Esineb 1 haiguses |
| TRAK1trafficking kinesin protein 1 | Pole registreeritud | Esineb 1 haiguses |
| ZFYVE26zinc finger FYVE-type containing 26 | 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