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Tunnus
Nerve damage causing decreased feeling and movement
Kliiniline nimetus: Sensorimotor neuropathy
Kokkuvõte
- Teised nimetused
- Mixed polyneuropathy, Sensorimotor peripheral neuropathy
- Kehasüsteem
- Abnormality of the nervous system
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Read the genes linked to Nerve damage causing decreased feeling and movement, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test107 geeni on seotud tunnusega Nerve damage causing decreased feeling and movement
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Nerve damage causing decreased feeling and movement. 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 |
|---|---|---|
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Alati | Esineb 2 haiguses |
| ARHGAP19Rho GTPase activating protein 19 | Alati | Esineb 1 haiguses |
| CLCF1cardiotrophin like cytokine factor 1 | Alati | Esineb 1 haiguses |
| COA3cytochrome c oxidase assembly factor 3 | Alati | Esineb 1 haiguses |
| GET4guided entry of tail-anchored proteins factor 4 | Alati | Esineb 1 haiguses |
| HMBShydroxymethylbilane synthase | Alati | Esineb 2 haiguses |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Alati | Esineb 1 haiguses |
| LAMA2laminin subunit alpha 2 | Alati | Esineb 2 haiguses |
| LITAFlipopolysaccharide induced TNF factor | Alati | Esineb 1 haiguses |
| MCM3APminichromosome maintenance complex component 3 associated protein | Alati | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Alati | Esineb 2 haiguses |
| RAB7ARAB7A, member RAS oncogene family | Alati | Esineb 1 haiguses |
| RCC1regulator of chromosome condensation 1 | Alati | Esineb 1 haiguses |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Alati | Esineb 1 haiguses |
| TYMPthymidine phosphorylase | Alati | Esineb 2 haiguses |
| XRCC1X-ray repair cross complementing 1 | Alati | Esineb 1 haiguses |
| ADA2adenosine deaminase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DHHdesert hedgehog signaling molecule | Väga sageli (80–99%) | Esineb 1 haiguses |
| GALCgalactosylceramidase | Väga sageli (80–99%) | Esineb 4 haiguses |
| GDAP1ganglioside induced differentiation associated protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LIG3DNA ligase 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MMEmembrane metalloendopeptidase | Väga sageli (80–99%) | Esineb 3 haiguses |
| NEFLneurofilament light chain | Väga sageli (80–99%) | Esineb 3 haiguses |
| NGLY1N-glycanase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PDK3pyruvate dehydrogenase kinase 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIK3R5phosphoinositide-3-kinase regulatory subunit 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PSAPprosaposin | Väga sageli (80–99%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Väga sageli (80–99%) | Esineb 2 haiguses |
| SETXsenataxin | Väga sageli (80–99%) | Esineb 1 haiguses |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Väga sageli (80–99%) | Esineb 1 haiguses |
| TFGtrafficking from ER to golgi regulator | Väga sageli (80–99%) | Esineb 1 haiguses |
| ABCD1ATP binding cassette subfamily D member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| AMACRalpha-methylacyl-CoA racemase | Sageli (30–79%) | Esineb 2 haiguses |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| COA8cytochrome c oxidase assembly factor 8 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAJC3DnaJ heat shock protein family (Hsp40) member C3 | Sageli (30–79%) | Esineb 1 haiguses |
| DNM1Ldynamin 1L | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 67 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| EMILIN1elastin microfibril interfacer 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GBA2glucosylceramidase beta 2 | Sageli (30–79%) | Esineb 1 haiguses |
| GJB1gap junction protein beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| IFRD1interferon related developmental regulator 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KIF1Akinesin family member 1A | Sageli (30–79%) | Esineb 2 haiguses |
| MPZmyelin protein zero | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Sageli (30–79%) | Esineb 1 haiguses |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Sageli (30–79%) | Esineb 2 haiguses |
| OPA1OPA1 mitochondrial dynamin like GTPase | Sageli (30–79%) | Esineb 2 haiguses |
| PEX6peroxisomal biogenesis factor 6 | Sageli (30–79%) | Esineb 1 haiguses |
| PLA2G6phospholipase A2 group VI | Sageli (30–79%) | Esineb 1 haiguses |
| PMP22peripheral myelin protein 22 | Sageli (30–79%) | Esineb 2 haiguses |
| PPIBpeptidylprolyl isomerase B | Sageli (30–79%) | Esineb 1 haiguses |
| RFC1replication factor C subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SACSsacsin molecular chaperone | Sageli (30–79%) | Esineb 1 haiguses |
| SCO2synthesis of cytochrome C oxidase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC25A46solute carrier family 25 member 46 | Sageli (30–79%) | Esineb 1 haiguses |
| TDP1tyrosyl-DNA phosphodiesterase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| UCHL1ubiquitin C-terminal hydrolase L1 | Sageli (30–79%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Sageli (30–79%) | Esineb 1 haiguses |
| VPS13Dvacuolar protein sorting 13 homolog D | Sageli (30–79%) | Esineb 1 haiguses |
| VPS41VPS41 subunit of HOPS complex | Sageli (30–79%) | Esineb 1 haiguses |
| VRK1VRK serine/threonine kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| AHCYadenosylhomocysteinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| B2Mbeta-2-microglobulin | Mõnikord (5–29%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIF5Akinesin family member 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| MRE11MRE11 double strand break repair nuclease | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PNKPpolynucleotide kinase 3'-phosphatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | Mõnikord (5–29%) | Esineb 2 haiguses |
| RNASEH1ribonuclease H1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RRM1ribonucleotide reductase catalytic subunit M1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCARB2scavenger receptor class B member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC30A10solute carrier family 30 member 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Harva (1–4%) | Esineb 1 haiguses |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Harva (1–4%) | Esineb 1 haiguses |
| ABHD12abhydrolase domain containing 12, lysophospholipase | Pole registreeritud | Esineb 1 haiguses |
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Pole registreeritud | Esineb 1 haiguses |
| FDX2ferredoxin 2 | Pole registreeritud | Esineb 1 haiguses |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Pole registreeritud | Esineb 1 haiguses |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Pole registreeritud | Esineb 1 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Pole registreeritud | Esineb 1 haiguses |
| NEFHneurofilament heavy chain | Pole registreeritud | Esineb 1 haiguses |
| PDYNprodynorphin | Pole registreeritud | Esineb 1 haiguses |
| PEX7peroxisomal biogenesis factor 7 | Pole registreeritud | Esineb 1 haiguses |
| PHYHphytanoyl-CoA 2-hydroxylase | Pole registreeritud | Esineb 1 haiguses |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Pole registreeritud | Esineb 1 haiguses |
| RPIAribose 5-phosphate isomerase A | Pole registreeritud | Esineb 1 haiguses |
| SCYL1SCY1 like pseudokinase 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC52A2solute carrier family 52 member 2 | 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.
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.
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Logi sisseKüsiAlustaalates 449 $
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast