ProfileGDS1065 / 207338_s_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 47% 38% 60% 64% 56% 53% 63% 60% 52% 56% 44% 59% 49% 61% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 139.647
GSM24653Normal subject 225.238
GSM24654Normal subject 380.460
GSM24655A3243G-MELAS subject 154.864
GSM24656A3243G-MELAS subject 259.356
GSM24657A3243G-MELAS subject 372.153
GSM24658A3243G-MELAS subject 469.563
GSM24659A3243G-PEO subject 154.560
GSM24660A3243G-PEO subject 244.152
GSM24661A3243G-PEO subject 34156
GSM24662A3243G-PEO subject 429.844
GSM24663mtDNA "Common"-deletion subject 166.259
GSM24664mtDNA "Common"-deletion subject 275.149
GSM24665mtDNA "Common"-deletion subject 3102.261
GSM24666mtDNA "Common"-deletion subject 4135.465