Træk
Incoordination
A deficit in coordination of muscle movements. Coordination is defined as the orchestrated movement of multiple body parts as required to accomplish intended actions, like walking.
Resumé
- Også kaldet
- Difficulties in coordination, Incoordination of limb movements, Limb incoordination, Poor coordination, Poor motor coordination
- 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 Test115 gener knyttet til Incoordination
Ændringer i disse gener forårsager sjældne tilstande, hvor Incoordination 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 |
|---|---|---|
| ABCA2ATP binding cassette subfamily A member 2 | Altid | I 1 tilstand |
| ATP9AATPase phospholipid transporting 9A | Altid | I 1 tilstand |
| CREBBPCREB binding lysine acetyltransferase | Altid | I 1 tilstand |
| EEF1A2eukaryotic translation elongation factor 1 alpha 2 | Altid | I 1 tilstand |
| EP300EP300 lysine acetyltransferase | Altid | I 1 tilstand |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Altid | I 1 tilstand |
| GRID2glutamate ionotropic receptor delta type subunit 2 | Altid | I 1 tilstand |
| JPH1junctophilin 1 | Altid | I 1 tilstand |
| LRRC7leucine rich repeat containing 7 | Altid | I 1 tilstand |
| MCCC1methylcrotonyl-CoA carboxylase subunit 1 | Altid | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Altid | I 1 tilstand |
| MSL2MSL complex subunit 2 | Altid | I 1 tilstand |
| NADK2NAD kinase 2, mitochondrial | Altid | I 1 tilstand |
| PANK2pantothenate kinase 2 | Altid | I 1 tilstand |
| PDE2Aphosphodiesterase 2A | Altid | I 1 tilstand |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Altid | I 1 tilstand |
| RNU2-2RNA, U2 small nuclear 2 | Altid | I 1 tilstand |
| RPIAribose 5-phosphate isomerase A | Altid | I 1 tilstand |
| RRP12ribosomal RNA processing 12 homolog | Altid | I 1 tilstand |
| SIN3ASIN3 transcription regulator family member A | Altid | I 1 tilstand |
| SLC18A2solute carrier family 18 member A2 | Altid | I 1 tilstand |
| TINF2TERF1 interacting nuclear factor 2 | Altid | I 1 tilstand |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Meget ofte (80–99 %) | I 2 tilstande |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Meget ofte (80–99 %) | I 2 tilstande |
| SPTBN2spectrin beta, non-erythrocytic 2 | Meget ofte (80–99 %) | I 2 tilstande |
| TXN2thioredoxin 2 | Meget ofte (80–99 %) | I 1 tilstand |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Ofte (30–79 %) | I 1 tilstand |
| CHAMP1chromosome alignment maintaining phosphoprotein 1 | Ofte (30–79 %) | I 1 tilstand |
| CPLX1complexin 1 | Ofte (30–79 %) | I 1 tilstand |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Ofte (30–79 %) | I 1 tilstand |
| ELNelastin | Ofte (30–79 %) | I 1 tilstand |
| GCDHglutaryl-CoA dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| GCH1GTP cyclohydrolase 1 | Ofte (30–79 %) | I 1 tilstand |
| HEXBhexosaminidase subunit beta | Ofte (30–79 %) | I 1 tilstand |
| LZTFL1leucine zipper transcription factor like 1 | Ofte (30–79 %) | I 1 tilstand |
| MLXIPLMLX interacting protein like | Ofte (30–79 %) | I 1 tilstand |
| MTFMTmitochondrial methionyl-tRNA formyltransferase | Ofte (30–79 %) | I 1 tilstand |
| PMPCApeptidase, mitochondrial processing subunit alpha | Ofte (30–79 %) | I 2 tilstande |
| RDH11retinol dehydrogenase 11 | Ofte (30–79 %) | I 1 tilstand |
| RFC4replication factor C subunit 4 | Ofte (30–79 %) | I 1 tilstand |
Vis 75 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| SCN8Asodium voltage-gated channel alpha subunit 8 | Ofte (30–79 %) | I 1 tilstand |
| SLC25A15solute carrier family 25 member 15 | Ofte (30–79 %) | I 2 tilstande |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Ofte (30–79 %) | I 1 tilstand |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Ofte (30–79 %) | I 1 tilstand |
| TANGO2transport and golgi organization 2 homolog | Ofte (30–79 %) | I 2 tilstande |
| TBC1D24TBC1 domain family member 24 | Ofte (30–79 %) | I 1 tilstand |
| TPRtranslocated promoter region, nuclear basket protein | Ofte (30–79 %) | I 1 tilstand |
| VPS13Avacuolar protein sorting 13 homolog A | Ofte (30–79 %) | I 1 tilstand |
| AASSaminoadipate-semialdehyde synthase | Nogle gange (5–29 %) | I 1 tilstand |
| ADGRV1adhesion G protein-coupled receptor V1 | Nogle gange (5–29 %) | I 1 tilstand |
| AFF2ALF transcription elongation factor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ALMS1ALMS1 centrosome and basal body associated protein | Nogle gange (5–29 %) | I 1 tilstand |
| APC2APC regulator of Wnt signaling pathway 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Nogle gange (5–29 %) | I 1 tilstand |
| CARS1cysteinyl-tRNA synthetase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CDC42BPBCDC42 binding protein kinase beta | Nogle gange (5–29 %) | I 1 tilstand |
| CPA6carboxypeptidase A6 | Nogle gange (5–29 %) | I 1 tilstand |
| FGF13fibroblast growth factor 13 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Nogle gange (5–29 %) | I 1 tilstand |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Nogle gange (5–29 %) | I 1 tilstand |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Nogle gange (5–29 %) | I 2 tilstande |
| GALTgalactose-1-phosphate uridylyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| GJB1gap junction protein beta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HCN1hyperpolarization activated cyclic nucleotide gated potassium channel 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HSD17B10hydroxysteroid 17-beta dehydrogenase 10 | Nogle gange (5–29 %) | I 1 tilstand |
| KCND3potassium voltage-gated channel subfamily D member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| LYSTlysosomal trafficking regulator | Nogle gange (5–29 %) | I 1 tilstand |
| MED13Lmediator complex subunit 13L | Nogle gange (5–29 %) | I 1 tilstand |
| MORC2MORC family CW-type zinc finger 2 | Nogle gange (5–29 %) | I 1 tilstand |
| NAA20N-alpha-acetyltransferase 20, NatB catalytic subunit | Nogle gange (5–29 %) | I 1 tilstand |
| NIPA1NIPA magnesium transporter 1 | Nogle gange (5–29 %) | I 1 tilstand |
| NIPA2NIPA magnesium transporter 2 | Nogle gange (5–29 %) | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Nogle gange (5–29 %) | I 2 tilstande |
| PCDH19protocadherin 19 | Nogle gange (5–29 %) | I 1 tilstand |
| PRNPprion protein (Kanno blood group) | Nogle gange (5–29 %) | I 2 tilstande |
| PRRT2proline rich transmembrane protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| RORARAR related orphan receptor A | Nogle gange (5–29 %) | I 1 tilstand |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Nogle gange (5–29 %) | I 2 tilstande |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Nogle gange (5–29 %) | I 2 tilstande |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Nogle gange (5–29 %) | I 2 tilstande |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Nogle gange (5–29 %) | I 2 tilstande |
| SETSET nuclear proto-oncogene | Nogle gange (5–29 %) | I 1 tilstand |
| SIM1SIM bHLH transcription factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC32A1solute carrier family 32 member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| STX1Bsyntaxin 1B | Nogle gange (5–29 %) | I 1 tilstand |
| TTC19tetratricopeptide repeat domain 19 | Nogle gange (5–29 %) | I 1 tilstand |
| TUBG1tubulin gamma 1 | Nogle gange (5–29 %) | I 1 tilstand |
| YWHAGtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma | Nogle gange (5–29 %) | I 1 tilstand |
| POGZpogo transposable element derived with ZNF domain | Sjældent (1–4%) | I 1 tilstand |
| ABCD1ATP binding cassette subfamily D member 1 | Ikke registreret | I 1 tilstand |
| ARL6ARF like GTPase 6 | Ikke registreret | I 1 tilstand |
| ATP7BATPase copper transporting beta | Ikke registreret | I 1 tilstand |
| ATXN10ataxin 10 | Ikke registreret | I 1 tilstand |
| ATXN8ataxin 8 | Ikke registreret | I 1 tilstand |
| ATXN8OSATXN8 opposite strand lncRNA | Ikke registreret | I 1 tilstand |
| BBS1Bardet-Biedl syndrome 1 | Ikke registreret | I 1 tilstand |
| BMPR1Bbone morphogenetic protein receptor type 1B | Ikke registreret | I 1 tilstand |
| CCDC28Bcoiled-coil domain containing 28B | Ikke registreret | I 1 tilstand |
| EEDembryonic ectoderm development | Ikke registreret | I 1 tilstand |
| EEF2eukaryotic translation elongation factor 2 | Ikke registreret | I 1 tilstand |
| ELP1elongator acetyltransferase complex subunit 1 | Ikke registreret | I 1 tilstand |
| FXNfrataxin | Ikke registreret | I 1 tilstand |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Ikke registreret | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Ikke registreret | I 1 tilstand |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Ikke registreret | I 1 tilstand |
| LMBRD1LMBR1 domain containing 1 | Ikke registreret | I 1 tilstand |
| MTHFRmethylenetetrahydrofolate reductase | Ikke registreret | I 1 tilstand |
| MTR5-methyltetrahydrofolate-homocysteine methyltransferase | Ikke registreret | I 1 tilstand |
| NOP56NOP56 ribonucleoprotein | Ikke registreret | I 1 tilstand |
| SPG21SPG21 abhydrolase domain containing, maspardin | Ikke registreret | I 1 tilstand |
| TBC1D23TBC1 domain family member 23 | Ikke registreret | I 1 tilstand |
| TCF20transcription factor 20 | Ikke registreret | I 1 tilstand |
| TCF4transcription factor 4 | Ikke registreret | I 1 tilstand |
| TGM6transglutaminase 6 | 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