ProfileGDS1065 / 205452_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 54% 54% 41% 61% 45% 54% 50% 60% 45% 54% 50% 42% 53% 47% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 152.454
GSM24653Normal subject 250.954
GSM24654Normal subject 334.641
GSM24655A3243G-MELAS subject 147.561
GSM24656A3243G-MELAS subject 238.545
GSM24657A3243G-MELAS subject 377.254
GSM24658A3243G-MELAS subject 439.550
GSM24659A3243G-PEO subject 154.460
GSM24660A3243G-PEO subject 234.645
GSM24661A3243G-PEO subject 337.354
GSM24662A3243G-PEO subject 437.150
GSM24663mtDNA "Common"-deletion subject 131.542
GSM24664mtDNA "Common"-deletion subject 290.353
GSM24665mtDNA "Common"-deletion subject 357.347
GSM24666mtDNA "Common"-deletion subject 460.148