Træk
Nerve damage causing decreased feeling and movement
Klinisk navn: Sensorimotor neuropathy
Resumé
- Også kaldet
- Mixed polyneuropathy, Sensorimotor peripheral neuropathy
- 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 Test107 gener knyttet til Nerve damage causing decreased feeling and movement
Ændringer i disse gener forårsager sjældne tilstande, hvor Nerve damage causing decreased feeling and 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 |
|---|---|---|
| AFG3L2AFG3 like matrix AAA peptidase subunit 2 | Altid | I 2 tilstande |
| ARHGAP19Rho GTPase activating protein 19 | Altid | I 1 tilstand |
| CLCF1cardiotrophin like cytokine factor 1 | Altid | I 1 tilstand |
| COA3cytochrome c oxidase assembly factor 3 | Altid | I 1 tilstand |
| GET4guided entry of tail-anchored proteins factor 4 | Altid | I 1 tilstand |
| HMBShydroxymethylbilane synthase | Altid | I 2 tilstande |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Altid | I 1 tilstand |
| LAMA2laminin subunit alpha 2 | Altid | I 2 tilstande |
| LITAFlipopolysaccharide induced TNF factor | Altid | I 1 tilstand |
| MCM3APminichromosome maintenance complex component 3 associated protein | Altid | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Altid | I 2 tilstande |
| RAB7ARAB7A, member RAS oncogene family | Altid | I 1 tilstand |
| RCC1regulator of chromosome condensation 1 | Altid | I 1 tilstand |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Altid | I 1 tilstand |
| TYMPthymidine phosphorylase | Altid | I 2 tilstande |
| XRCC1X-ray repair cross complementing 1 | Altid | I 1 tilstand |
| ADA2adenosine deaminase 2 | Meget ofte (80–99 %) | I 1 tilstand |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Meget ofte (80–99 %) | I 1 tilstand |
| DHHdesert hedgehog signaling molecule | Meget ofte (80–99 %) | I 1 tilstand |
| GALCgalactosylceramidase | Meget ofte (80–99 %) | I 4 tilstande |
| GDAP1ganglioside induced differentiation associated protein 1 | Meget ofte (80–99 %) | I 1 tilstand |
| LIG3DNA ligase 3 | Meget ofte (80–99 %) | I 1 tilstand |
| MMEmembrane metalloendopeptidase | Meget ofte (80–99 %) | I 3 tilstande |
| NEFLneurofilament light chain | Meget ofte (80–99 %) | I 3 tilstande |
| NGLY1N-glycanase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| PDK3pyruvate dehydrogenase kinase 3 | Meget ofte (80–99 %) | I 1 tilstand |
| PIK3R5phosphoinositide-3-kinase regulatory subunit 5 | Meget ofte (80–99 %) | I 1 tilstand |
| PSAPprosaposin | Meget ofte (80–99 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Meget ofte (80–99 %) | I 2 tilstande |
| SETXsenataxin | Meget ofte (80–99 %) | I 1 tilstand |
| SH3TC2SH3 domain and tetratricopeptide repeats 2 | Meget ofte (80–99 %) | I 1 tilstand |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Meget ofte (80–99 %) | I 1 tilstand |
| TFGtrafficking from ER to golgi regulator | Meget ofte (80–99 %) | I 1 tilstand |
| ABCD1ATP binding cassette subfamily D member 1 | Ofte (30–79 %) | I 1 tilstand |
| AMACRalpha-methylacyl-CoA racemase | Ofte (30–79 %) | I 2 tilstande |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| COA8cytochrome c oxidase assembly factor 8 | Ofte (30–79 %) | I 1 tilstand |
| DNAJC3DnaJ heat shock protein family (Hsp40) member C3 | Ofte (30–79 %) | I 1 tilstand |
| DNM1Ldynamin 1L | Ofte (30–79 %) | I 1 tilstand |
Vis 67 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| EMILIN1elastin microfibril interfacer 1 | Ofte (30–79 %) | I 1 tilstand |
| GBA2glucosylceramidase beta 2 | Ofte (30–79 %) | I 1 tilstand |
| GJB1gap junction protein beta 1 | Ofte (30–79 %) | I 1 tilstand |
| IFRD1interferon related developmental regulator 1 | Ofte (30–79 %) | I 1 tilstand |
| KIF1Akinesin family member 1A | Ofte (30–79 %) | I 2 tilstande |
| MPZmyelin protein zero | Ofte (30–79 %) | I 1 tilstand |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Ofte (30–79 %) | I 2 tilstande |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Ofte (30–79 %) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Ofte (30–79 %) | I 2 tilstande |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Ofte (30–79 %) | I 2 tilstande |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Ofte (30–79 %) | I 2 tilstande |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Ofte (30–79 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Ofte (30–79 %) | I 2 tilstande |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Ofte (30–79 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Ofte (30–79 %) | I 2 tilstande |
| OPA1OPA1 mitochondrial dynamin like GTPase | Ofte (30–79 %) | I 2 tilstande |
| PEX6peroxisomal biogenesis factor 6 | Ofte (30–79 %) | I 1 tilstand |
| PLA2G6phospholipase A2 group VI | Ofte (30–79 %) | I 1 tilstand |
| PMP22peripheral myelin protein 22 | Ofte (30–79 %) | I 2 tilstande |
| PPIBpeptidylprolyl isomerase B | Ofte (30–79 %) | I 1 tilstand |
| RFC1replication factor C subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| SACSsacsin molecular chaperone | Ofte (30–79 %) | I 1 tilstand |
| SCO2synthesis of cytochrome C oxidase 2 | Ofte (30–79 %) | I 1 tilstand |
| SLC25A46solute carrier family 25 member 46 | Ofte (30–79 %) | I 1 tilstand |
| TDP1tyrosyl-DNA phosphodiesterase 1 | Ofte (30–79 %) | I 1 tilstand |
| UCHL1ubiquitin C-terminal hydrolase L1 | Ofte (30–79 %) | I 1 tilstand |
| VCPvalosin containing protein | Ofte (30–79 %) | I 1 tilstand |
| VPS13Dvacuolar protein sorting 13 homolog D | Ofte (30–79 %) | I 1 tilstand |
| VPS41VPS41 subunit of HOPS complex | Ofte (30–79 %) | I 1 tilstand |
| VRK1VRK serine/threonine kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| AHCYadenosylhomocysteinase | Nogle gange (5–29 %) | I 1 tilstand |
| B2Mbeta-2-microglobulin | Nogle gange (5–29 %) | I 1 tilstand |
| GBA1glucosylceramidase beta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KIF5Akinesin family member 5A | Nogle gange (5–29 %) | I 1 tilstand |
| MRE11MRE11 double strand break repair nuclease | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Nogle gange (5–29 %) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Nogle gange (5–29 %) | I 1 tilstand |
| PNKPpolynucleotide kinase 3'-phosphatase | Nogle gange (5–29 %) | I 1 tilstand |
| PPP2R2Bprotein phosphatase 2 regulatory subunit Bbeta | Nogle gange (5–29 %) | I 2 tilstande |
| RNASEH1ribonuclease H1 | Nogle gange (5–29 %) | I 1 tilstand |
| RRM1ribonucleotide reductase catalytic subunit M1 | Nogle gange (5–29 %) | I 1 tilstand |
| SCARB2scavenger receptor class B member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC30A10solute carrier family 30 member 10 | Nogle gange (5–29 %) | I 1 tilstand |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Sjældent (1–4%) | I 1 tilstand |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Sjældent (1–4%) | I 1 tilstand |
| ABHD12abhydrolase domain containing 12, lysophospholipase | Ikke registreret | I 1 tilstand |
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Ikke registreret | I 1 tilstand |
| FDX2ferredoxin 2 | Ikke registreret | I 1 tilstand |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Ikke registreret | I 1 tilstand |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Ikke registreret | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Ikke registreret | I 1 tilstand |
| NEFHneurofilament heavy chain | Ikke registreret | I 1 tilstand |
| PDYNprodynorphin | Ikke registreret | I 1 tilstand |
| PEX7peroxisomal biogenesis factor 7 | Ikke registreret | I 1 tilstand |
| PHYHphytanoyl-CoA 2-hydroxylase | Ikke registreret | I 1 tilstand |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Ikke registreret | I 1 tilstand |
| RPIAribose 5-phosphate isomerase A | Ikke registreret | I 1 tilstand |
| SCYL1SCY1 like pseudokinase 1 | Ikke registreret | I 1 tilstand |
| SLC52A2solute carrier family 52 member 2 | 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.
Bredere træk
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.
Én test. Svar for hele livet.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger