Egenskap
Fiber type grouping
An abnormal distribution of muscle fiber types in muscle tissue. Human skeletal muscle contains at least two fiber types recognizable by histochemical techniques. In transverse sections of normal skeletal muscle, type 1 and type 2 fibers are distributed in a random fashion. Grouping of fibers of the same type can be seen in certain peripheral neuropathies, thought to be due to reinnervation of denervated muscle fibers by sprouting axons. With grouping, motor units enlarge. The fibers of a motor unit, which are normally scattered, come to lie adjacent to one another. Histochemical examination shows groups of muscle fibers of the same histochemical type.
Sammanfattning
- Även kallad
- Fibre type grouping
- Kroppssystem
- Abnormality of the musculoskeletal system
Den här sidan som data
Lägg till .json i sidans adress, eller begär application/json, för att läsa den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/fiber-type-grouping.json"
page <- fromJSON(url)
page$trait$nameLäs generna kopplade till Fiber type grouping, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test19 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Spinal Muscular AtrophyReads 3 of these genesEMILIN1HSPB8REEP1About this report →
- Myofibrillar MyopathiesReads 2 of these genesHSPB8BAG3About this report →
- Inherited Neurodegenerative DisordersReads 9 of these genesDARS2EMILIN1HSPB8REEP1SPTLC1POLGAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesEMILIN1HSPB8REEP1SPTLC1GDAP1POLGAbout this report →
Show 15 more reports
- Charcot-Marie-Tooth DiseaseReads 4 of these genesEMILIN1HSPB8REEP1GDAP1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesSPTLC1ANXA11About this report →
- Cutis LaxaReads 1 of these genesEMILIN1About this report →
- Distal MyopathiesReads 1 of these genesLRP12About this report →
- Congenital MyopathiesReads 1 of these genesTPM2About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesSPTLC1About this report →
- Congenital Muscular DystrophiesReads 1 of these genesCOL6A1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesCOL6A1About this report →
- Primary Mitochondrial DiseaseReads 2 of these genesPOLGTWNKAbout this report →
- Dilated CardiomyopathyReads 1 of these genesBAG3About this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTWNKAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesREEP1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesDARS2About this report →
- Hearing Loss and DeafnessReads 1 of these genesMYH14About this report →
Läs generna kopplade till Fiber type grouping, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test17 gener kopplade till Fiber type grouping
Förändringar i dessa gener orsakar sällsynta tillstånd där Fiber type grouping förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| COL6A1collagen type VI alpha 1 chain | Alltid | I 1 tillstånd |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Alltid | I 1 tillstånd |
| EMILIN1elastin microfibril interfacer 1 | Alltid | I 1 tillstånd |
| HSPB8heat shock protein family B (small) member 8 | Alltid | I 1 tillstånd |
| MYH14myosin heavy chain 14 | Alltid | I 1 tillstånd |
| REEP1receptor accessory protein 1 | Alltid | I 1 tillstånd |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Alltid | I 1 tillstånd |
| WSB2WD repeat and SOCS box containing 2 | Alltid | I 1 tillstånd |
| YME1L1YME1 like 1 ATPase | Alltid | I 1 tillstånd |
| BAG3BAG cochaperone 3 | Ofta (30–79 %) | I 1 tillstånd |
| GDAP1ganglioside induced differentiation associated protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| LRP12LDL receptor related protein 12 | Ofta (30–79 %) | I 1 tillstånd |
| POLGDNA polymerase gamma, catalytic subunit | Ofta (30–79 %) | I 1 tillstånd |
| SLC5A6solute carrier family 5 member 6 | Ofta (30–79 %) | I 1 tillstånd |
| TWNKtwinkle mtDNA helicase | Ofta (30–79 %) | I 2 tillstånd |
| TPM2tropomyosin 2 | Ibland (5–29 %) | I 1 tillstånd |
| ANXA11annexin A11 | Inte registrerat | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
Bredare egenskaper
Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.18-8b139e39.
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