Egenskap
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.
Sammendrag
- Kroppssystem
- Abnormality of the nervous system
ReferansegenomGRCh38hg38
Posisjoner på gen- og variantsidene følger dette valget i denne nettleseren.
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Få mitt Genome Test179 gener knyttet til Lack of coordination of movement
Endringer i disse genene forårsaker sjeldne tilstander der Lack of coordination of movement 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 |
|---|---|---|
| ABCB7ATP binding cassette subfamily B member 7 | Alltid | I 2 tilstander |
| ACBD5acyl-CoA binding domain containing 5 | Alltid | I 1 tilstand |
| ADGRG1adhesion G protein-coupled receptor G1 | Alltid | I 2 tilstander |
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Alltid | I 2 tilstander |
| ATG5autophagy related 5 | Alltid | I 1 tilstand |
| ATXN7ataxin 7 | Alltid | I 2 tilstander |
| BAIAP2BAR/IMD domain containing adaptor protein 2 | Alltid | I 1 tilstand |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Alltid | I 1 tilstand |
| CCDC88Ccoiled-coil and HOOK domain protein 88C | Alltid | I 2 tilstander |
| CHP1calcineurin like EF-hand protein 1 | Alltid | I 1 tilstand |
| COA7cytochrome c oxidase assembly factor 7 | Alltid | I 1 tilstand |
| COG8component of oligomeric golgi complex 8 | Alltid | I 1 tilstand |
| COQ4coenzyme Q4 | Alltid | I 1 tilstand |
| CRATcarnitine O-acetyltransferase | Alltid | I 1 tilstand |
| CTSAcathepsin A | Alltid | I 1 tilstand |
| CWF19L1CWF19 like cell cycle control factor 1 | Alltid | I 2 tilstander |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Alltid | I 1 tilstand |
| FEM1Bfem-1 homolog B | Alltid | I 1 tilstand |
| GFAPglial fibrillary acidic protein | Alltid | I 1 tilstand |
| GPAA1glycosylphosphatidylinositol anchor attachment 1 | Alltid | I 2 tilstander |
| GRID2glutamate ionotropic receptor delta type subunit 2 | Alltid | I 1 tilstand |
| GRM1glutamate metabotropic receptor 1 | Alltid | I 3 tilstander |
| GTPBP2GTP binding protein 2 | Alltid | I 1 tilstand |
| HIBCH3-hydroxyisobutyryl-CoA hydrolase | Alltid | I 1 tilstand |
| HTRA1HtrA serine peptidase 1 | Alltid | I 1 tilstand |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Alltid | I 1 tilstand |
| KIF1Ckinesin family member 1C | Alltid | I 2 tilstander |
| MAGmyelin associated glycoprotein | Alltid | I 2 tilstander |
| MALmal, T cell differentiation protein (MAL blood group) | Alltid | I 1 tilstand |
| MMADHCmetabolism of cobalamin associated D | Alltid | I 1 tilstand |
| OFD1OFD1 centriole and centriolar satellite protein | Alltid | I 1 tilstand |
| PIK3R5phosphoinositide-3-kinase regulatory subunit 5 | Alltid | I 1 tilstand |
| PMPCApeptidase, mitochondrial processing subunit alpha | Alltid | I 2 tilstander |
| PNPLA8patatin like domain 8, phospholipase A2 | Alltid | I 1 tilstand |
| POLR3BRNA polymerase III subunit B | Alltid | I 2 tilstander |
| PRDM13PR/SET domain 13 | Alltid | I 1 tilstand |
| PTRH2peptidyl-tRNA hydrolase 2 | Alltid | I 2 tilstander |
| RFC4replication factor C subunit 4 | Alltid | I 1 tilstand |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Alltid | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Alltid | I 1 tilstand |
Vis 139 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| SLC9A1solute carrier family 9 member A1 | Alltid | I 1 tilstand |
| SPARTspartin | Alltid | I 1 tilstand |
| SPTBN2spectrin beta, non-erythrocytic 2 | Alltid | I 3 tilstander |
| TGM6transglutaminase 6 | Alltid | I 2 tilstander |
| TOP3ADNA topoisomerase III alpha | Alltid | I 1 tilstand |
| TPP1tripeptidyl peptidase 1 | Alltid | I 2 tilstander |
| TTPAalpha tocopherol transfer protein | Alltid | I 2 tilstander |
| UROC1urocanate hydratase 1 | Alltid | I 1 tilstand |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Alltid | I 2 tilstander |
| XRCC1X-ray repair cross complementing 1 | Alltid | I 1 tilstand |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Svært ofte (80–99 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Svært ofte (80–99 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Svært ofte (80–99 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Svært ofte (80–99 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Svært ofte (80–99 %) | I 1 tilstand |
| ELNelastin | Svært ofte (80–99 %) | I 1 tilstand |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Svært ofte (80–99 %) | I 1 tilstand |
| FMR1fragile X messenger ribonucleoprotein 1 | Svært ofte (80–99 %) | I 2 tilstander |
| GTF2Igeneral transcription factor IIi | Svært ofte (80–99 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Svært ofte (80–99 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Svært ofte (80–99 %) | I 1 tilstand |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Svært ofte (80–99 %) | I 2 tilstander |
| LIMK1LIM domain kinase 1 | Svært ofte (80–99 %) | I 1 tilstand |
| METTL27methyltransferase like 27 | Svært ofte (80–99 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Svært ofte (80–99 %) | I 1 tilstand |
| RFC2replication factor C subunit 2 | Svært ofte (80–99 %) | I 1 tilstand |
| STX1Asyntaxin 1A | Svært ofte (80–99 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Svært ofte (80–99 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Svært ofte (80–99 %) | I 1 tilstand |
| VPS37DVPS37D subunit of ESCRT-I | Svært ofte (80–99 %) | I 1 tilstand |
| ANO10anoctamin 10 | Ofte (30–79 %) | I 2 tilstander |
| 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 tilstander |
| CAMTA1calmodulin binding transcription activator 1 | Ofte (30–79 %) | I 2 tilstander |
| 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 tilstander |
| FXNfrataxin | Ofte (30–79 %) | I 1 tilstand |
| GJB1gap junction protein beta 1 | Ofte (30–79 %) | I 2 tilstander |
| IFRD1interferon related developmental regulator 1 | Ofte (30–79 %) | I 1 tilstand |
| KIF1Akinesin family member 1A | Ofte (30–79 %) | I 2 tilstander |
| 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 tilstander |
| MRE11MRE11 double strand break repair nuclease | Ofte (30–79 %) | I 2 tilstander |
| MSTO1misato mitochondrial distribution and morphology regulator 1 | Ofte (30–79 %) | I 2 tilstander |
| 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 tilstander |
| PEX16peroxisomal biogenesis factor 16 | Ofte (30–79 %) | I 1 tilstand |
| PI4KAphosphatidylinositol 4-kinase alpha | Ofte (30–79 %) | I 2 tilstander |
| 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 tilstander |
| POLR3ARNA polymerase III subunit A | Ofte (30–79 %) | I 2 tilstander |
| POU4F1POU class 4 homeobox 1 | Ofte (30–79 %) | I 2 tilstander |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Ofte (30–79 %) | I 1 tilstand |
| RARS1arginyl-tRNA synthetase 1 | Ofte (30–79 %) | I 2 tilstander |
| 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 tilstander |
| SAMD9Lsterile alpha motif domain containing 9 like | Ofte (30–79 %) | I 2 tilstander |
| 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 tilstander |
| 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 | Noen ganger (5–29 %) | I 1 tilstand |
| ABCD1ATP binding cassette subfamily D member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ADPRSADP-ribosylserine hydrolase | Noen ganger (5–29 %) | I 1 tilstand |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Noen ganger (5–29 %) | I 1 tilstand |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Noen ganger (5–29 %) | I 1 tilstand |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| ATXN1ataxin 1 | Noen ganger (5–29 %) | I 2 tilstander |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Noen ganger (5–29 %) | I 1 tilstand |
| CLN5CLN5 lysosomal BMP synthase | Noen ganger (5–29 %) | I 1 tilstand |
| CTDP1CTD phosphatase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| FTH1ferritin heavy chain 1 | Noen ganger (5–29 %) | I 1 tilstand |
| IVDisovaleryl-CoA dehydrogenase | Noen ganger (5–29 %) | I 1 tilstand |
| LIG3DNA ligase 3 | Noen ganger (5–29 %) | I 1 tilstand |
| LMNB1lamin B1 | Noen ganger (5–29 %) | I 1 tilstand |
| LRPPRCleucine rich pentatricopeptide repeat containing | Noen ganger (5–29 %) | I 1 tilstand |
| MTTPmicrosomal triglyceride transfer protein | Noen ganger (5–29 %) | I 1 tilstand |
| NEU1neuraminidase 1 | Noen ganger (5–29 %) | I 3 tilstander |
| PMPCBpeptidase, mitochondrial processing subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| PRNPprion protein (Kanno blood group) | Noen ganger (5–29 %) | I 2 tilstander |
| RNASEH1ribonuclease H1 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC25A46solute carrier family 25 member 46 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC5A6solute carrier family 5 member 6 | Noen ganger (5–29 %) | I 1 tilstand |
| SMC5structural maintenance of chromosomes 5 | Noen ganger (5–29 %) | I 1 tilstand |
| SRPX2sushi repeat containing protein X-linked 2 | Noen ganger (5–29 %) | I 1 tilstand |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Noen ganger (5–29 %) | I 2 tilstander |
| TMEM106Btransmembrane protein 106B | Noen ganger (5–29 %) | I 1 tilstand |
| TMEM63Atransmembrane protein 63A | Noen ganger (5–29 %) | I 1 tilstand |
| TTC19tetratricopeptide repeat domain 19 | Noen ganger (5–29 %) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Noen ganger (5–29 %) | I 1 tilstand |
| LAMP2lysosome associated membrane protein 2 | Sjelden (1–4%) | I 1 tilstand |
| ABHD12abhydrolase domain containing 12, lysophospholipase | Ikke registrert | I 1 tilstand |
| ATXN2ataxin 2 | Ikke registrert | I 1 tilstand |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Ikke registrert | I 1 tilstand |
| BRAT1BRCA1 associated ATM activator 1 | Ikke registrert | I 1 tilstand |
| CACNA2D2calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Ikke registrert | I 1 tilstand |
| CAV1caveolin 1 | Ikke registrert | I 1 tilstand |
| DEGS1delta 4-desaturase, sphingolipid 1 | Ikke registrert | I 1 tilstand |
| GJC2gap junction protein gamma 2 | Ikke registrert | I 1 tilstand |
| IRF2BPLinterferon regulatory factor 2 binding protein like | Ikke registrert | I 1 tilstand |
| MYORGmyogenesis regulating glycosidase | Ikke registrert | I 1 tilstand |
| NDUFAF2NADH:ubiquinone oxidoreductase complex assembly factor 2 | Ikke registrert | I 1 tilstand |
| NFASCneurofascin | Ikke registrert | I 1 tilstand |
| NGLY1N-glycanase 1 | Ikke registrert | I 1 tilstand |
| PEX2peroxisomal biogenesis factor 2 | Ikke registrert | I 1 tilstand |
| PLA2G6phospholipase A2 group VI | Ikke registrert | I 1 tilstand |
| PLD3phospholipase D family member 3 | Ikke registrert | I 1 tilstand |
| PLP1proteolipid protein 1 | Ikke registrert | I 1 tilstand |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | Ikke registrert | I 1 tilstand |
| PRICKLE1prickle planar cell polarity protein 1 | Ikke registrert | I 1 tilstand |
| PRKCGprotein kinase C gamma | Ikke registrert | I 1 tilstand |
| SQSTM1sequestosome 1 | Ikke registrert | I 1 tilstand |
| STUB1STIP1 homology and U-box containing protein 1 | Ikke registrert | I 1 tilstand |
| TBPTATA-box binding protein | Ikke registrert | I 1 tilstand |
| TCTN2tectonic family member 2 | Ikke registrert | I 1 tilstand |
| UCHL1ubiquitin C-terminal hydrolase L1 | Ikke registrert | I 1 tilstand |
| VLDLRvery low density lipoprotein receptor | Ikke registrert | I 1 tilstand |
| VWA3Bvon Willebrand factor A domain containing 3B | Ikke registrert | I 1 tilstand |
| WDR81WD repeat domain 81 | Ikke registrert | I 1 tilstand |
| XRCC4X-ray repair cross complementing 4 | 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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