Tunnus
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.
Kokkuvõte
- Teised nimetused
- Difficulties in coordination, Incoordination of limb movements, Limb incoordination, Poor coordination, Poor motor coordination
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Incoordination, and the rest of your genome, with one test.
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Telli oma Genome Test115 geeni on seotud tunnusega Incoordination
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Incoordination. 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 |
|---|---|---|
| ABCA2ATP binding cassette subfamily A member 2 | Alati | Esineb 1 haiguses |
| ATP9AATPase phospholipid transporting 9A | Alati | Esineb 1 haiguses |
| CREBBPCREB binding lysine acetyltransferase | Alati | Esineb 1 haiguses |
| EEF1A2eukaryotic translation elongation factor 1 alpha 2 | Alati | Esineb 1 haiguses |
| EP300EP300 lysine acetyltransferase | Alati | Esineb 1 haiguses |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Alati | Esineb 1 haiguses |
| GRID2glutamate ionotropic receptor delta type subunit 2 | Alati | Esineb 1 haiguses |
| JPH1junctophilin 1 | Alati | Esineb 1 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| MCCC1methylcrotonyl-CoA carboxylase subunit 1 | Alati | Esineb 1 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Alati | Esineb 1 haiguses |
| MSL2MSL complex subunit 2 | Alati | Esineb 1 haiguses |
| NADK2NAD kinase 2, mitochondrial | Alati | Esineb 1 haiguses |
| PANK2pantothenate kinase 2 | Alati | Esineb 1 haiguses |
| PDE2Aphosphodiesterase 2A | Alati | Esineb 1 haiguses |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Alati | Esineb 1 haiguses |
| RNU2-2RNA, U2 small nuclear 2 | Alati | Esineb 1 haiguses |
| RPIAribose 5-phosphate isomerase A | Alati | Esineb 1 haiguses |
| RRP12ribosomal RNA processing 12 homolog | Alati | Esineb 1 haiguses |
| SIN3ASIN3 transcription regulator family member A | Alati | Esineb 1 haiguses |
| SLC18A2solute carrier family 18 member A2 | Alati | Esineb 1 haiguses |
| TINF2TERF1 interacting nuclear factor 2 | Alati | Esineb 1 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Väga sageli (80–99%) | Esineb 2 haiguses |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SPTBN2spectrin beta, non-erythrocytic 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TXN2thioredoxin 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Sageli (30–79%) | Esineb 1 haiguses |
| CHAMP1chromosome alignment maintaining phosphoprotein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CPLX1complexin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Sageli (30–79%) | Esineb 1 haiguses |
| ELNelastin | Sageli (30–79%) | Esineb 1 haiguses |
| GCDHglutaryl-CoA dehydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| GCH1GTP cyclohydrolase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HEXBhexosaminidase subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| LZTFL1leucine zipper transcription factor like 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MLXIPLMLX interacting protein like | Sageli (30–79%) | Esineb 1 haiguses |
| MTFMTmitochondrial methionyl-tRNA formyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| PMPCApeptidase, mitochondrial processing subunit alpha | Sageli (30–79%) | Esineb 2 haiguses |
| RDH11retinol dehydrogenase 11 | Sageli (30–79%) | Esineb 1 haiguses |
| RFC4replication factor C subunit 4 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 75 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SCN8Asodium voltage-gated channel alpha subunit 8 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC25A15solute carrier family 25 member 15 | Sageli (30–79%) | Esineb 2 haiguses |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Sageli (30–79%) | Esineb 1 haiguses |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TANGO2transport and golgi organization 2 homolog | Sageli (30–79%) | Esineb 2 haiguses |
| TBC1D24TBC1 domain family member 24 | Sageli (30–79%) | Esineb 1 haiguses |
| TPRtranslocated promoter region, nuclear basket protein | Sageli (30–79%) | Esineb 1 haiguses |
| VPS13Avacuolar protein sorting 13 homolog A | Sageli (30–79%) | Esineb 1 haiguses |
| AASSaminoadipate-semialdehyde synthase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ADGRV1adhesion G protein-coupled receptor V1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| AFF2ALF transcription elongation factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALMS1ALMS1 centrosome and basal body associated protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| APC2APC regulator of Wnt signaling pathway 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CARS1cysteinyl-tRNA synthetase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDC42BPBCDC42 binding protein kinase beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| CPA6carboxypeptidase A6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FGF13fibroblast growth factor 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Mõnikord (5–29%) | Esineb 1 haiguses |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| GALTgalactose-1-phosphate uridylyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJB1gap junction protein beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HCN1hyperpolarization activated cyclic nucleotide gated potassium channel 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HSD17B10hydroxysteroid 17-beta dehydrogenase 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCND3potassium voltage-gated channel subfamily D member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LYSTlysosomal trafficking regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| MED13Lmediator complex subunit 13L | Mõnikord (5–29%) | Esineb 1 haiguses |
| MORC2MORC family CW-type zinc finger 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAA20N-alpha-acetyltransferase 20, NatB catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| NIPA1NIPA magnesium transporter 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NIPA2NIPA magnesium transporter 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NKX2-1NK2 homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NSD1nuclear receptor binding SET domain protein 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| PCDH19protocadherin 19 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRNPprion protein (Kanno blood group) | Mõnikord (5–29%) | Esineb 2 haiguses |
| PRRT2proline rich transmembrane protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RORARAR related orphan receptor A | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SETSET nuclear proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| SIM1SIM bHLH transcription factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC32A1solute carrier family 32 member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STX1Bsyntaxin 1B | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTC19tetratricopeptide repeat domain 19 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TUBG1tubulin gamma 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| YWHAGtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma | Mõnikord (5–29%) | Esineb 1 haiguses |
| POGZpogo transposable element derived with ZNF domain | Harva (1–4%) | Esineb 1 haiguses |
| ABCD1ATP binding cassette subfamily D member 1 | Pole registreeritud | Esineb 1 haiguses |
| ARL6ARF like GTPase 6 | Pole registreeritud | Esineb 1 haiguses |
| ATP7BATPase copper transporting beta | Pole registreeritud | Esineb 1 haiguses |
| ATXN10ataxin 10 | Pole registreeritud | Esineb 1 haiguses |
| ATXN8ataxin 8 | Pole registreeritud | Esineb 1 haiguses |
| ATXN8OSATXN8 opposite strand lncRNA | Pole registreeritud | Esineb 1 haiguses |
| BBS1Bardet-Biedl syndrome 1 | Pole registreeritud | Esineb 1 haiguses |
| BMPR1Bbone morphogenetic protein receptor type 1B | Pole registreeritud | Esineb 1 haiguses |
| CCDC28Bcoiled-coil domain containing 28B | Pole registreeritud | Esineb 1 haiguses |
| EEDembryonic ectoderm development | Pole registreeritud | Esineb 1 haiguses |
| EEF2eukaryotic translation elongation factor 2 | Pole registreeritud | Esineb 1 haiguses |
| ELP1elongator acetyltransferase complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| FXNfrataxin | Pole registreeritud | Esineb 1 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Pole registreeritud | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Pole registreeritud | Esineb 1 haiguses |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Pole registreeritud | Esineb 1 haiguses |
| LMBRD1LMBR1 domain containing 1 | Pole registreeritud | Esineb 1 haiguses |
| MTHFRmethylenetetrahydrofolate reductase | Pole registreeritud | Esineb 1 haiguses |
| MTR5-methyltetrahydrofolate-homocysteine methyltransferase | Pole registreeritud | Esineb 1 haiguses |
| NOP56NOP56 ribonucleoprotein | Pole registreeritud | Esineb 1 haiguses |
| SPG21SPG21 abhydrolase domain containing, maspardin | Pole registreeritud | Esineb 1 haiguses |
| TBC1D23TBC1 domain family member 23 | Pole registreeritud | Esineb 1 haiguses |
| TCF20transcription factor 20 | Pole registreeritud | Esineb 1 haiguses |
| TCF4transcription factor 4 | Pole registreeritud | Esineb 1 haiguses |
| TGM6transglutaminase 6 | 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