ProfileGDS1065 / 204008_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 55% 62% 64% 40% 34% 49% 51% 45% 33% 46% 45% 45% 44% 31% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 153.855
GSM24653Normal subject 268.662
GSM24654Normal subject 397.464
GSM24655A3243G-MELAS subject 122.340
GSM24656A3243G-MELAS subject 22434
GSM24657A3243G-MELAS subject 361.349
GSM24658A3243G-MELAS subject 44151
GSM24659A3243G-PEO subject 131.445
GSM24660A3243G-PEO subject 219.533
GSM24661A3243G-PEO subject 326.246
GSM24662A3243G-PEO subject 430.445
GSM24663mtDNA "Common"-deletion subject 137.345
GSM24664mtDNA "Common"-deletion subject 261.244
GSM24665mtDNA "Common"-deletion subject 327.831
GSM24666mtDNA "Common"-deletion subject 449.243