ProfileGDS1065 / 200969_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 66% 67% 52% 53% 61% 73% 66% 64% 60% 61% 71% 63% 63% 62% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 185.766
GSM24653Normal subject 286.467
GSM24654Normal subject 357.652
GSM24655A3243G-MELAS subject 136.253
GSM24656A3243G-MELAS subject 272.361
GSM24657A3243G-MELAS subject 3193.673
GSM24658A3243G-MELAS subject 480.966
GSM24659A3243G-PEO subject 163.564
GSM24660A3243G-PEO subject 26060
GSM24661A3243G-PEO subject 348.161
GSM24662A3243G-PEO subject 491.571
GSM24663mtDNA "Common"-deletion subject 179.163
GSM24664mtDNA "Common"-deletion subject 2134.563
GSM24665mtDNA "Common"-deletion subject 3109.162
GSM24666mtDNA "Common"-deletion subject 4188.171