ProfileGDS1065 / 206169_x_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 68% 63% 42% 59% 65% 70% 65% 76% 71% 80% 85% 65% 58% 53% 77% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19868
GSM24653Normal subject 270.963
GSM24654Normal subject 337.542
GSM24655A3243G-MELAS subject 14459
GSM24656A3243G-MELAS subject 284.965
GSM24657A3243G-MELAS subject 3158.570
GSM24658A3243G-MELAS subject 477.265
GSM24659A3243G-PEO subject 110676
GSM24660A3243G-PEO subject 297.271
GSM24661A3243G-PEO subject 3119.880
GSM24662A3243G-PEO subject 420285
GSM24663mtDNA "Common"-deletion subject 185.165
GSM24664mtDNA "Common"-deletion subject 2106.858
GSM24665mtDNA "Common"-deletion subject 373.953
GSM24666mtDNA "Common"-deletion subject 4251.677