ProfileGDS1065 / 217961_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 88% 89% 84% 85% 86% 89% 86% 90% 89% 86% 90% 88% 89% 85% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1339.688
GSM24653Normal subject 233589
GSM24654Normal subject 330084
GSM24655A3243G-MELAS subject 1156.885
GSM24656A3243G-MELAS subject 2260.986
GSM24657A3243G-MELAS subject 358789
GSM24658A3243G-MELAS subject 4265.186
GSM24659A3243G-PEO subject 1280.690
GSM24660A3243G-PEO subject 2300.789
GSM24661A3243G-PEO subject 3191.186
GSM24662A3243G-PEO subject 4326.390
GSM24663mtDNA "Common"-deletion subject 1343.988
GSM24664mtDNA "Common"-deletion subject 2639.189
GSM24665mtDNA "Common"-deletion subject 3396.985
GSM24666mtDNA "Common"-deletion subject 4527.787