ProfileGDS1065 / 204086_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 17% 52% 43% 43% 51% 34% 35% 35% 34% 14% 31% 46% 38% 37% 32% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.417
GSM24653Normal subject 246.252
GSM24654Normal subject 339.243
GSM24655A3243G-MELAS subject 124.743
GSM24656A3243G-MELAS subject 249.851
GSM24657A3243G-MELAS subject 330.534
GSM24658A3243G-MELAS subject 419.835
GSM24659A3243G-PEO subject 120.635
GSM24660A3243G-PEO subject 22034
GSM24661A3243G-PEO subject 34.314
GSM24662A3243G-PEO subject 416.431
GSM24663mtDNA "Common"-deletion subject 138.846
GSM24664mtDNA "Common"-deletion subject 247.638
GSM24665mtDNA "Common"-deletion subject 337.437
GSM24666mtDNA "Common"-deletion subject 428.232