ProfileGDS1065 / 207220_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 44% 18% 23% 38% 45% 34% 30% 20% 37% 42% 32% 40% 37% 35% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 134.844
GSM24653Normal subject 27.618
GSM24654Normal subject 312.423
GSM24655A3243G-MELAS subject 120.338
GSM24656A3243G-MELAS subject 239.545
GSM24657A3243G-MELAS subject 330.734
GSM24658A3243G-MELAS subject 414.630
GSM24659A3243G-PEO subject 18.920
GSM24660A3243G-PEO subject 223.437
GSM24661A3243G-PEO subject 322.642
GSM24662A3243G-PEO subject 416.632
GSM24663mtDNA "Common"-deletion subject 12940
GSM24664mtDNA "Common"-deletion subject 24637
GSM24665mtDNA "Common"-deletion subject 333.235
GSM24666mtDNA "Common"-deletion subject 445.441