BaseSpace
Import Your Data
QuickView

FAQ

More QuickView FAQs

Back to top
Clear Search sequence regions
(e.g. PBX1, G-protein-coupled receptor binding, HIV infection, Kidney, Prozac, rs2300478)
Bookmark Forward

QuickView for mitochondrial disease (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. CPS1
  2. SCO2
  3. MSTO1
  4. UQCRH
  5. PUS1
  1. No SNPs found
Explore Genetic Markers Results

Pathway Enrichment

Most Correlated Biogroups

  1. MOOTHA_VOXPHOS
  2. WONG_MITOCHONDRIA_GENE_MODULE
  3. RNA binding
  4. DANG_BOUND_BY_MYC
  5. cellular respiration
Explore Pathway Enrichment Results

Curated Studies

Most Correlated Studies

  1. Skeletal muscle expression profiling in mitochondrial disorders
  2. Mouse Phenotypes - Autosomal recessive hereditary disorder
  3. OMIM - Metabolic diseases
  4. Blood expression profile of MELAS syndrome patients
  5. OMIM - Eye Related Disorders
Explore Curated Studies Results

Literature

Most Relevant Literature

  1. Role of creatine as biomarker of mitochondrial diseases.
  2. Mitochondrial diseases and epilepsy.
  3. Mitochondrial disease--an important cause of end-stage renal failure.
  4. Mechanisms of mitochondrial diseases.
  5. Design and implementation of the first randomized controlled trial of coenzyme CoQ₁₀ in children wit…
Explore Literature Results

Clinical Trials

Most Relevant Clinical Trials

  1. Applying pGz in Mitochondrial Disease
  2. Survey on Supplement Use in Mitochondrial Disease
  3. GDF-15 as a Biomarker for Mitochondrial Disease
  4. Glycemic Index in Mitochondrial Disease
  5. Anesthetic Effects in Mitochondrial Disease
Explore Clinical Trials Results
  • Copyright © 2024 Illumina Inc. All rights reserved.