ProfileGDS1065 / 202205_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 53% 26% 43% 47% 54% 49% 50% 49% 55% 50% 51% 56% 52% 55% 49% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149.953
GSM24653Normal subject 213.426
GSM24654Normal subject 339.543
GSM24655A3243G-MELAS subject 128.547
GSM24656A3243G-MELAS subject 25654
GSM24657A3243G-MELAS subject 362.249
GSM24658A3243G-MELAS subject 440.250
GSM24659A3243G-PEO subject 135.749
GSM24660A3243G-PEO subject 251.255
GSM24661A3243G-PEO subject 330.950
GSM24662A3243G-PEO subject 439.451
GSM24663mtDNA "Common"-deletion subject 158.556
GSM24664mtDNA "Common"-deletion subject 283.452
GSM24665mtDNA "Common"-deletion subject 379.455
GSM24666mtDNA "Common"-deletion subject 462.449