Træk
Lack of coordination of movement
Klinisk navn: Dysmetria
A type of ataxia characterized by the inability to carry out movements with the correct range and motion across the plane of more than one joint related to incorrect estimation of the distances required for targeted movements.
Resumé
- 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 Test179 gener knyttet til Lack of coordination of movement
Ændringer i disse gener forårsager sjældne tilstande, hvor Lack of coordination of movement 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 |
|---|---|---|
| ABCB7ATP binding cassette subfamily B member 7 | Altid | I 2 tilstande |
| ACBD5acyl-CoA binding domain containing 5 | Altid | I 1 tilstand |
| ADGRG1adhesion G protein-coupled receptor G1 | Altid | I 2 tilstande |
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Altid | I 2 tilstande |
| ATG5autophagy related 5 | Altid | I 1 tilstand |
| ATXN7ataxin 7 | Altid | I 2 tilstande |
| BAIAP2BAR/IMD domain containing adaptor protein 2 | Altid | I 1 tilstand |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Altid | I 1 tilstand |
| CCDC88Ccoiled-coil and HOOK domain protein 88C | Altid | I 2 tilstande |
| CHP1calcineurin like EF-hand protein 1 | Altid | I 1 tilstand |
| COA7cytochrome c oxidase assembly factor 7 | Altid | I 1 tilstand |
| COG8component of oligomeric golgi complex 8 | Altid | I 1 tilstand |
| COQ4coenzyme Q4 | Altid | I 1 tilstand |
| CRATcarnitine O-acetyltransferase | Altid | I 1 tilstand |
| CTSAcathepsin A | Altid | I 1 tilstand |
| CWF19L1CWF19 like cell cycle control factor 1 | Altid | I 2 tilstande |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Altid | I 1 tilstand |
| FEM1Bfem-1 homolog B | Altid | I 1 tilstand |
| GFAPglial fibrillary acidic protein | Altid | I 1 tilstand |
| GPAA1glycosylphosphatidylinositol anchor attachment 1 | Altid | I 2 tilstande |
| GRID2glutamate ionotropic receptor delta type subunit 2 | Altid | I 1 tilstand |
| GRM1glutamate metabotropic receptor 1 | Altid | I 3 tilstande |
| GTPBP2GTP binding protein 2 | Altid | I 1 tilstand |
| HIBCH3-hydroxyisobutyryl-CoA hydrolase | Altid | I 1 tilstand |
| HTRA1HtrA serine peptidase 1 | Altid | I 1 tilstand |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Altid | I 1 tilstand |
| KIF1Ckinesin family member 1C | Altid | I 2 tilstande |
| MAGmyelin associated glycoprotein | Altid | I 2 tilstande |
| MALmal, T cell differentiation protein (MAL blood group) | Altid | I 1 tilstand |
| MMADHCmetabolism of cobalamin associated D | Altid | I 1 tilstand |
| OFD1OFD1 centriole and centriolar satellite protein | Altid | I 1 tilstand |
| PIK3R5phosphoinositide-3-kinase regulatory subunit 5 | Altid | I 1 tilstand |
| PMPCApeptidase, mitochondrial processing subunit alpha | Altid | I 2 tilstande |
| PNPLA8patatin like domain 8, phospholipase A2 | Altid | I 1 tilstand |
| POLR3BRNA polymerase III subunit B | Altid | I 2 tilstande |
| PRDM13PR/SET domain 13 | Altid | I 1 tilstand |
| PTRH2peptidyl-tRNA hydrolase 2 | Altid | I 2 tilstande |
| RFC4replication factor C subunit 4 | Altid | I 1 tilstand |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Altid | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Altid | I 1 tilstand |
Vis 139 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| SLC9A1solute carrier family 9 member A1 | Altid | I 1 tilstand |
| SPARTspartin | Altid | I 1 tilstand |
| SPTBN2spectrin beta, non-erythrocytic 2 | Altid | I 3 tilstande |
| TGM6transglutaminase 6 | Altid | I 2 tilstande |
| TOP3ADNA topoisomerase III alpha | Altid | I 1 tilstand |
| TPP1tripeptidyl peptidase 1 | Altid | I 2 tilstande |
| TTPAalpha tocopherol transfer protein | Altid | I 2 tilstande |
| UROC1urocanate hydratase 1 | Altid | I 1 tilstand |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Altid | I 2 tilstande |
| XRCC1X-ray repair cross complementing 1 | Altid | I 1 tilstand |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Meget ofte (80–99 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Meget ofte (80–99 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Meget ofte (80–99 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Meget ofte (80–99 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Meget ofte (80–99 %) | I 1 tilstand |
| ELNelastin | Meget ofte (80–99 %) | I 1 tilstand |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Meget ofte (80–99 %) | I 1 tilstand |
| FMR1fragile X messenger ribonucleoprotein 1 | Meget ofte (80–99 %) | I 2 tilstande |
| GTF2Igeneral transcription factor IIi | Meget ofte (80–99 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Meget ofte (80–99 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Meget ofte (80–99 %) | I 1 tilstand |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Meget ofte (80–99 %) | I 2 tilstande |
| LIMK1LIM domain kinase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| METTL27methyltransferase like 27 | Meget ofte (80–99 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Meget ofte (80–99 %) | I 1 tilstand |
| RFC2replication factor C subunit 2 | Meget ofte (80–99 %) | I 1 tilstand |
| STX1Asyntaxin 1A | Meget ofte (80–99 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Meget ofte (80–99 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Meget ofte (80–99 %) | I 1 tilstand |
| VPS37DVPS37D subunit of ESCRT-I | Meget ofte (80–99 %) | I 1 tilstand |
| ANO10anoctamin 10 | Ofte (30–79 %) | I 2 tilstande |
| AP5Z1adaptor related protein complex 5 subunit zeta 1 | Ofte (30–79 %) | I 1 tilstand |
| ATN1atrophin 1 | Ofte (30–79 %) | I 1 tilstand |
| ATXN10ataxin 10 | Ofte (30–79 %) | I 2 tilstande |
| CAMTA1calmodulin binding transcription activator 1 | Ofte (30–79 %) | I 2 tilstande |
| CAPN1calpain 1 | Ofte (30–79 %) | I 1 tilstand |
| COQ5coenzyme Q5, methyltransferase | Ofte (30–79 %) | I 1 tilstand |
| EBF3EBF transcription factor 3 | Ofte (30–79 %) | I 1 tilstand |
| ELOVL1ELOVL fatty acid elongase 1 | Ofte (30–79 %) | I 1 tilstand |
| ERMARDER membrane associated RNA degradation | Ofte (30–79 %) | I 1 tilstand |
| EXOSC5exosome component 5 | Ofte (30–79 %) | I 1 tilstand |
| FA2Hfatty acid 2-hydroxylase | Ofte (30–79 %) | I 2 tilstande |
| FXNfrataxin | Ofte (30–79 %) | I 1 tilstand |
| GJB1gap junction protein beta 1 | Ofte (30–79 %) | I 2 tilstande |
| IFRD1interferon related developmental regulator 1 | Ofte (30–79 %) | I 1 tilstand |
| KIF1Akinesin family member 1A | Ofte (30–79 %) | I 2 tilstande |
| LAGE3L antigen family member 3 | Ofte (30–79 %) | I 1 tilstand |
| LNPKlunapark, ER junction formation factor | Ofte (30–79 %) | I 1 tilstand |
| MARS2methionyl-tRNA synthetase 2, mitochondrial | Ofte (30–79 %) | I 2 tilstande |
| MRE11MRE11 double strand break repair nuclease | Ofte (30–79 %) | I 2 tilstande |
| MSTO1misato mitochondrial distribution and morphology regulator 1 | Ofte (30–79 %) | I 2 tilstande |
| NOP56NOP56 ribonucleoprotein | Ofte (30–79 %) | I 1 tilstand |
| OGDHoxoglutarate dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| OPA1OPA1 mitochondrial dynamin like GTPase | Ofte (30–79 %) | I 1 tilstand |
| PDYNprodynorphin | Ofte (30–79 %) | I 2 tilstande |
| PEX16peroxisomal biogenesis factor 16 | Ofte (30–79 %) | I 1 tilstand |
| PI4KAphosphatidylinositol 4-kinase alpha | Ofte (30–79 %) | I 2 tilstande |
| PITRM1pitrilysin metallopeptidase 1 | Ofte (30–79 %) | I 1 tilstand |
| PMM2phosphomannomutase 2 | Ofte (30–79 %) | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Ofte (30–79 %) | I 3 tilstande |
| POLR3ARNA polymerase III subunit A | Ofte (30–79 %) | I 2 tilstande |
| POU4F1POU class 4 homeobox 1 | Ofte (30–79 %) | I 2 tilstande |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Ofte (30–79 %) | I 1 tilstand |
| RARS1arginyl-tRNA synthetase 1 | Ofte (30–79 %) | I 2 tilstande |
| REPS1RALBP1 associated Eps domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| RFC1replication factor C subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| RUSC2RUN and SH3 domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| SACSsacsin molecular chaperone | Ofte (30–79 %) | I 2 tilstande |
| SAMD9Lsterile alpha motif domain containing 9 like | Ofte (30–79 %) | I 2 tilstande |
| SFXN4sideroflexin 4 | Ofte (30–79 %) | I 1 tilstand |
| SHMT2serine hydroxymethyltransferase 2 | Ofte (30–79 %) | I 1 tilstand |
| SLC13A3solute carrier family 13 member 3 | Ofte (30–79 %) | I 1 tilstand |
| SLC25A15solute carrier family 25 member 15 | Ofte (30–79 %) | I 1 tilstand |
| SLC7A6OSsolute carrier family 7 member 6 opposite strand | Ofte (30–79 %) | I 1 tilstand |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Ofte (30–79 %) | I 1 tilstand |
| TECPR2tectonin beta-propeller repeat containing 2 | Ofte (30–79 %) | I 2 tilstande |
| TIMMDC1translocase of inner mitochondrial membrane domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| TSPOAP1TSPO associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| TUBA4Atubulin alpha 4a | Ofte (30–79 %) | I 1 tilstand |
| YME1L1YME1 like 1 ATPase | Ofte (30–79 %) | I 1 tilstand |
| AASSaminoadipate-semialdehyde synthase | Nogle gange (5–29 %) | I 1 tilstand |
| ABCD1ATP binding cassette subfamily D member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ADPRSADP-ribosylserine hydrolase | Nogle gange (5–29 %) | I 1 tilstand |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Nogle gange (5–29 %) | I 1 tilstand |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ATXN1ataxin 1 | Nogle gange (5–29 %) | I 2 tilstande |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Nogle gange (5–29 %) | I 1 tilstand |
| CLN5CLN5 lysosomal BMP synthase | Nogle gange (5–29 %) | I 1 tilstand |
| CTDP1CTD phosphatase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| FTH1ferritin heavy chain 1 | Nogle gange (5–29 %) | I 1 tilstand |
| IVDisovaleryl-CoA dehydrogenase | Nogle gange (5–29 %) | I 1 tilstand |
| LIG3DNA ligase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| LMNB1lamin B1 | Nogle gange (5–29 %) | I 1 tilstand |
| LRPPRCleucine rich pentatricopeptide repeat containing | Nogle gange (5–29 %) | I 1 tilstand |
| MTTPmicrosomal triglyceride transfer protein | Nogle gange (5–29 %) | I 1 tilstand |
| NEU1neuraminidase 1 | Nogle gange (5–29 %) | I 3 tilstande |
| PMPCBpeptidase, mitochondrial processing subunit beta | Nogle gange (5–29 %) | I 1 tilstand |
| PRNPprion protein (Kanno blood group) | Nogle gange (5–29 %) | I 2 tilstande |
| RNASEH1ribonuclease H1 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC25A46solute carrier family 25 member 46 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC5A6solute carrier family 5 member 6 | Nogle gange (5–29 %) | I 1 tilstand |
| SMC5structural maintenance of chromosomes 5 | Nogle gange (5–29 %) | I 1 tilstand |
| SRPX2sushi repeat containing protein X-linked 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Nogle gange (5–29 %) | I 2 tilstande |
| TMEM106Btransmembrane protein 106B | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM63Atransmembrane protein 63A | Nogle gange (5–29 %) | I 1 tilstand |
| TTC19tetratricopeptide repeat domain 19 | Nogle gange (5–29 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Nogle gange (5–29 %) | I 1 tilstand |
| LAMP2lysosome associated membrane protein 2 | Sjældent (1–4%) | I 1 tilstand |
| ABHD12abhydrolase domain containing 12, lysophospholipase | Ikke registreret | I 1 tilstand |
| ATXN2ataxin 2 | Ikke registreret | I 1 tilstand |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Ikke registreret | I 1 tilstand |
| BRAT1BRCA1 associated ATM activator 1 | Ikke registreret | I 1 tilstand |
| CACNA2D2calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Ikke registreret | I 1 tilstand |
| CAV1caveolin 1 | Ikke registreret | I 1 tilstand |
| DEGS1delta 4-desaturase, sphingolipid 1 | Ikke registreret | I 1 tilstand |
| GJC2gap junction protein gamma 2 | Ikke registreret | I 1 tilstand |
| IRF2BPLinterferon regulatory factor 2 binding protein like | Ikke registreret | I 1 tilstand |
| MYORGmyogenesis regulating glycosidase | Ikke registreret | I 1 tilstand |
| NDUFAF2NADH:ubiquinone oxidoreductase complex assembly factor 2 | Ikke registreret | I 1 tilstand |
| NFASCneurofascin | Ikke registreret | I 1 tilstand |
| NGLY1N-glycanase 1 | Ikke registreret | I 1 tilstand |
| PEX2peroxisomal biogenesis factor 2 | Ikke registreret | I 1 tilstand |
| PLA2G6phospholipase A2 group VI | Ikke registreret | I 1 tilstand |
| PLD3phospholipase D family member 3 | Ikke registreret | I 1 tilstand |
| PLP1proteolipid protein 1 | Ikke registreret | I 1 tilstand |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | Ikke registreret | I 1 tilstand |
| PRICKLE1prickle planar cell polarity protein 1 | Ikke registreret | I 1 tilstand |
| PRKCGprotein kinase C gamma | Ikke registreret | I 1 tilstand |
| SQSTM1sequestosome 1 | Ikke registreret | I 1 tilstand |
| STUB1STIP1 homology and U-box containing protein 1 | Ikke registreret | I 1 tilstand |
| TBPTATA-box binding protein | Ikke registreret | I 1 tilstand |
| TCTN2tectonic family member 2 | Ikke registreret | I 1 tilstand |
| UCHL1ubiquitin C-terminal hydrolase L1 | Ikke registreret | I 1 tilstand |
| VLDLRvery low density lipoprotein receptor | Ikke registreret | I 1 tilstand |
| VWA3Bvon Willebrand factor A domain containing 3B | Ikke registreret | I 1 tilstand |
| WDR81WD repeat domain 81 | Ikke registreret | I 1 tilstand |
| XRCC4X-ray repair cross complementing 4 | Ikke registreret | I 1 tilstand |
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.
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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.
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Fra 449 $Gratis forsendelse · Resultater på 6–8 uger