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Egenskap
Muscle spasm
Sudden and involuntary contractions of one or more muscles.
Sammendrag
- Også kalt
- Muscle cramps, Muscle spasms
- Kroppssystem
- Abnormality of the musculoskeletal system
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/muscle-spasm.json"
page <- fromJSON(url)
page$trait$nameMuscle spasmHP:0003394
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Les genene knyttet til Muscle spasm, og resten av genomet ditt, med én test.
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Få mitt Genome Test173 gener knyttet til Muscle spasm
Endringer i disse genene forårsaker sjeldne tilstander der Muscle spasm forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ARHGAP19Rho GTPase activating protein 19 | Alltid | I 1 tilstand |
| CASRcalcium sensing receptor | Alltid | I 1 tilstand |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Alltid | I 2 tilstander |
| COL4A1collagen type IV alpha 1 chain | Alltid | I 2 tilstander |
| FDX2ferredoxin 2 | Alltid | I 1 tilstand |
| HSPB8heat shock protein family B (small) member 8 | Alltid | I 1 tilstand |
| LRP12LDL receptor related protein 12 | Alltid | I 2 tilstander |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Alltid | I 4 tilstander |
| AMPD1adenosine monophosphate deaminase 1 | Svært ofte (80–99 %) | I 1 tilstand |
| AMPD3adenosine monophosphate deaminase 3 | Svært ofte (80–99 %) | I 1 tilstand |
| CASQ1calsequestrin 1 | Svært ofte (80–99 %) | I 2 tilstander |
| ORAI1ORAI calcium release-activated calcium modulator 1 | Svært ofte (80–99 %) | I 1 tilstand |
| STIM1stromal interaction molecule 1 | Svært ofte (80–99 %) | I 2 tilstander |
| VAPBVAMP associated protein B and C | Svært ofte (80–99 %) | I 4 tilstander |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Ofte (30–79 %) | I 1 tilstand |
| ANGangiogenin | Ofte (30–79 %) | I 1 tilstand |
| ANXA11annexin A11 | Ofte (30–79 %) | I 1 tilstand |
| ATXN1ataxin 1 | Ofte (30–79 %) | I 1 tilstand |
| ATXN2ataxin 2 | Ofte (30–79 %) | I 2 tilstander |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Ofte (30–79 %) | I 2 tilstander |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Ofte (30–79 %) | I 1 tilstand |
| CCNFcyclin F | Ofte (30–79 %) | I 1 tilstand |
| CFAP410cilia and flagella associated protein 410 | Ofte (30–79 %) | I 1 tilstand |
| CHMP2Bcharged multivesicular body protein 2B | Ofte (30–79 %) | I 1 tilstand |
| COL1A1collagen type I alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COL5A1collagen type V alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COL5A2collagen type V alpha 2 chain | Ofte (30–79 %) | I 1 tilstand |
| CRPPACDP-L-ribitol pyrophosphorylase A | Ofte (30–79 %) | I 1 tilstand |
| DAOD-amino acid oxidase | Ofte (30–79 %) | I 1 tilstand |
| DCTN1dynactin subunit 1 | Ofte (30–79 %) | I 2 tilstander |
| DMDdystrophin | Ofte (30–79 %) | I 2 tilstander |
| DNA2DNA replication helicase/nuclease 2 | Ofte (30–79 %) | I 2 tilstander |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Ofte (30–79 %) | I 1 tilstand |
| FIG4FIG4 phosphoinositide 5-phosphatase | Ofte (30–79 %) | I 1 tilstand |
| FKRPfukutin related protein | Ofte (30–79 %) | I 3 tilstander |
| FKTNfukutin | Ofte (30–79 %) | I 1 tilstand |
| FUSFUS RNA binding protein | Ofte (30–79 %) | I 1 tilstand |
| FXNfrataxin | Ofte (30–79 %) | I 1 tilstand |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Ofte (30–79 %) | I 1 tilstand |
| GLE1GLE1 RNA export mediator | Ofte (30–79 %) | I 1 tilstand |
Vis 133 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| GLT8D1glycosyltransferase 8 domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| GNA11G protein subunit alpha 11 | Ofte (30–79 %) | I 1 tilstand |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Ofte (30–79 %) | I 2 tilstander |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Ofte (30–79 %) | I 1 tilstand |
| HHAThedgehog acyltransferase | Ofte (30–79 %) | I 1 tilstand |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Ofte (30–79 %) | I 1 tilstand |
| HPDL4-hydroxyphenylpyruvate dioxygenase like | Ofte (30–79 %) | I 1 tilstand |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Ofte (30–79 %) | I 1 tilstand |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Ofte (30–79 %) | I 1 tilstand |
| KYkyphoscoliosis peptidase | Ofte (30–79 %) | I 1 tilstand |
| MATR3matrin 3 | Ofte (30–79 %) | I 1 tilstand |
| MFN2mitofusin 2 | Ofte (30–79 %) | I 1 tilstand |
| MICU1mitochondrial calcium uptake 1 | Ofte (30–79 %) | I 1 tilstand |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Ofte (30–79 %) | I 1 tilstand |
| NEFHneurofilament heavy chain | Ofte (30–79 %) | I 2 tilstander |
| NEK1NIMA related kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| OPA3outer mitochondrial membrane lipid metabolism regulator OPA3 | Ofte (30–79 %) | I 1 tilstand |
| OPTNoptineurin | Ofte (30–79 %) | I 1 tilstand |
| PFN1profilin 1 | Ofte (30–79 %) | I 1 tilstand |
| PGK1phosphoglycerate kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| POMT1protein O-mannosyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| PRPHperipherin | Ofte (30–79 %) | I 2 tilstander |
| PUS7pseudouridine synthase 7 | Ofte (30–79 %) | I 1 tilstand |
| RTN2reticulon 2 | Ofte (30–79 %) | I 1 tilstand |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Ofte (30–79 %) | I 1 tilstand |
| SMN1survival of motor neuron 1, telomeric | Ofte (30–79 %) | I 1 tilstand |
| SMN2survival of motor neuron 2, centromeric | Ofte (30–79 %) | I 1 tilstand |
| SOD1superoxide dismutase 1 | Ofte (30–79 %) | I 2 tilstander |
| SQSTM1sequestosome 1 | Ofte (30–79 %) | I 1 tilstand |
| STT3ASTT3 oligosaccharyltransferase complex catalytic subunit A | Ofte (30–79 %) | I 1 tilstand |
| SVILsupervillin | Ofte (30–79 %) | I 1 tilstand |
| TAF15TATA-box binding protein associated factor 15 | Ofte (30–79 %) | I 1 tilstand |
| TARDBPTAR DNA binding protein | Ofte (30–79 %) | I 1 tilstand |
| TBK1TANK binding kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC11trafficking protein particle complex subunit 11 | Ofte (30–79 %) | I 2 tilstander |
| TREM2triggering receptor expressed on myeloid cells 2 | Ofte (30–79 %) | I 1 tilstand |
| UBAP1ubiquitin associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| UBQLN2ubiquilin 2 | Ofte (30–79 %) | I 1 tilstand |
| UNC13Aunc-13 homolog A | Ofte (30–79 %) | I 1 tilstand |
| VCPvalosin containing protein | Ofte (30–79 %) | I 3 tilstander |
| WASHC5WASH complex subunit 5 | Ofte (30–79 %) | I 1 tilstand |
| ACADMacyl-CoA dehydrogenase medium chain | Noen ganger (5–29 %) | I 1 tilstand |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Noen ganger (5–29 %) | I 1 tilstand |
| ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunit | Noen ganger (5–29 %) | I 1 tilstand |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| ATXN3ataxin 3 | Noen ganger (5–29 %) | I 4 tilstander |
| BAG3BAG cochaperone 3 | Noen ganger (5–29 %) | I 1 tilstand |
| CADM3cell adhesion molecule 3 | Noen ganger (5–29 %) | I 1 tilstand |
| CLCN1chloride voltage-gated channel 1 | Noen ganger (5–29 %) | I 1 tilstand |
| CLCNKBchloride voltage-gated channel Kb | Noen ganger (5–29 %) | I 1 tilstand |
| CMPK2cytidine/uridine monophosphate kinase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| CPT2carnitine palmitoyltransferase 2 | Noen ganger (5–29 %) | I 2 tilstander |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DGUOKdeoxyguanosine kinase | Noen ganger (5–29 %) | I 1 tilstand |
| DLDdihydrolipoamide dehydrogenase | Noen ganger (5–29 %) | I 1 tilstand |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Noen ganger (5–29 %) | I 1 tilstand |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Noen ganger (5–29 %) | I 1 tilstand |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Noen ganger (5–29 %) | I 1 tilstand |
| FLVCR1FLVCR choline and heme transporter 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GALCgalactosylceramidase | Noen ganger (5–29 %) | I 1 tilstand |
| GBA1glucosylceramidase beta 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GBE11,4-alpha-glucan branching enzyme 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GFM2GTP dependent ribosome recycling factor mitochondrial 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GFPT1glutamine--fructose-6-phosphate transaminase 1 | Noen ganger (5–29 %) | I 3 tilstander |
| GIGYF2GRB10 interacting GYF protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GMPPBGDP-mannose pyrophosphorylase B | Noen ganger (5–29 %) | I 2 tilstander |
| GNASGNAS complex locus | Noen ganger (5–29 %) | I 3 tilstander |
| HEXBhexosaminidase subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| HSPB1heat shock protein family B (small) member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| HTRA2HtrA serine peptidase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| JAM2junctional adhesion molecule 2 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNE3potassium voltage-gated channel subfamily E regulatory subunit 3 | Noen ganger (5–29 %) | I 1 tilstand |
| KPNA3karyopherin subunit alpha 3 | Noen ganger (5–29 %) | I 1 tilstand |
| LPIN1lipin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| LRRK2leucine rich repeat kinase 2 | Noen ganger (5–29 %) | I 2 tilstander |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Noen ganger (5–29 %) | I 1 tilstand |
| MORC2MORC family CW-type zinc finger 2 | Noen ganger (5–29 %) | I 2 tilstander |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Noen ganger (5–29 %) | I 1 tilstand |
| MYORGmyogenesis regulating glycosidase | Noen ganger (5–29 %) | I 1 tilstand |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| NEFLneurofilament light chain | Noen ganger (5–29 %) | I 1 tilstand |
| OBSCNobscurin, cytoskeletal calmodulin and titin-interacting RhoGEF | Noen ganger (5–29 %) | I 1 tilstand |
| PARK7Parkinsonism associated deglycase | Noen ganger (5–29 %) | I 1 tilstand |
| PDGFBplatelet derived growth factor subunit B | Noen ganger (5–29 %) | I 1 tilstand |
| PDGFRBplatelet derived growth factor receptor beta | Noen ganger (5–29 %) | I 1 tilstand |
| PHKA1phosphorylase kinase regulatory subunit alpha 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PHKBphosphorylase kinase regulatory subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| PHKG1phosphorylase kinase catalytic subunit gamma 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Noen ganger (5–29 %) | I 1 tilstand |
| PINK1PTEN induced kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PMP22peripheral myelin protein 22 | Noen ganger (5–29 %) | I 1 tilstand |
| PODXLpodocalyxin like | Noen ganger (5–29 %) | I 1 tilstand |
| PRKNparkin RBR E3 ubiquitin protein ligase | Noen ganger (5–29 %) | I 1 tilstand |
| PSAPprosaposin | Noen ganger (5–29 %) | I 1 tilstand |
| RNASEH1ribonuclease H1 | Noen ganger (5–29 %) | I 1 tilstand |
| RRP12ribosomal RNA processing 12 homolog | Noen ganger (5–29 %) | I 1 tilstand |
| SLC12A3solute carrier family 12 member 3 | Noen ganger (5–29 %) | I 2 tilstander |
| SLC20A2solute carrier family 20 member 2 | Noen ganger (5–29 %) | I 1 tilstand |
| SNCAsynuclein alpha | Noen ganger (5–29 %) | I 2 tilstander |
| STX16syntaxin 16 | Noen ganger (5–29 %) | I 1 tilstand |
| SYNJ1synaptojanin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| UCHL1ubiquitin C-terminal hydrolase L1 | Noen ganger (5–29 %) | I 1 tilstand |
| VPS13Cvacuolar protein sorting 13 homolog C | Noen ganger (5–29 %) | I 1 tilstand |
| VPS35VPS35 retromer complex component | Noen ganger (5–29 %) | I 1 tilstand |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ACADVLacyl-CoA dehydrogenase very long chain | Sjelden (1–4%) | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Sjelden (1–4%) | I 1 tilstand |
| POLG2DNA polymerase gamma 2, accessory subunit | Sjelden (1–4%) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sjelden (1–4%) | I 1 tilstand |
| SLC25A4solute carrier family 25 member 4 | Sjelden (1–4%) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Sjelden (1–4%) | I 1 tilstand |
| ABCB6ATP binding cassette subfamily B member 6 (LAN blood group) | Ikke registrert | I 1 tilstand |
| ARandrogen receptor | Ikke registrert | I 1 tilstand |
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Ikke registrert | I 1 tilstand |
| CAV3caveolin 3 | Ikke registrert | I 1 tilstand |
| CHRNEcholinergic receptor nicotinic epsilon subunit | Ikke registrert | I 1 tilstand |
| DOK7docking protein 7 | Ikke registrert | I 1 tilstand |
| FBXO38F-box protein 38 | Ikke registrert | I 1 tilstand |
| GBF1golgi brefeldin A resistant guanine nucleotide exchange factor 1 | Ikke registrert | I 1 tilstand |
| GLAgalactosidase alpha | Ikke registrert | I 1 tilstand |
| HINT1histidine triad nucleotide binding protein 1 | Ikke registrert | I 1 tilstand |
| ISCUiron-sulfur cluster assembly enzyme | Ikke registrert | I 1 tilstand |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Ikke registrert | I 1 tilstand |
| LDHAlactate dehydrogenase A | Ikke registrert | I 1 tilstand |
| MUSKmuscle associated receptor tyrosine kinase | Ikke registrert | I 1 tilstand |
| SLC12A1solute carrier family 12 member 1 | Ikke registrert | I 1 tilstand |
| TFGtrafficking from ER to golgi regulator | Ikke registrert | I 1 tilstand |
| TRPM6transient receptor potential cation channel subfamily M member 6 | Ikke registrert | I 1 tilstand |
| TRPM7transient receptor potential cation channel subfamily M member 7 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
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Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.16-c6eea6bf.
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Logg innSpørKom i gangfra 449 $
Én test. En livstid med svar.
Fra 449 $Gratis frakt · Resultater på 6–8 uker