ProfileGDS1065 / 209235_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 50% 22% 38% 33% 26% 52% 50% 25% 20% 29% 45% 26% 19% 42% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14450
GSM24653Normal subject 210.222
GSM24654Normal subject 330.138
GSM24655A3243G-MELAS subject 115.733
GSM24656A3243G-MELAS subject 215.526
GSM24657A3243G-MELAS subject 369.652
GSM24658A3243G-MELAS subject 440.350
GSM24659A3243G-PEO subject 111.525
GSM24660A3243G-PEO subject 28.720
GSM24661A3243G-PEO subject 311.129
GSM24662A3243G-PEO subject 431.445
GSM24663mtDNA "Common"-deletion subject 113.326
GSM24664mtDNA "Common"-deletion subject 21519
GSM24665mtDNA "Common"-deletion subject 34742
GSM24666mtDNA "Common"-deletion subject 448.643