ProfileGDS1065 / 221738_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 58% 44% 53% 52% 47% 49% 46% 47% 58% 62% 47% 62% 54% 50% 40% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16358
GSM24653Normal subject 233.144
GSM24654Normal subject 359.753
GSM24655A3243G-MELAS subject 135.352
GSM24656A3243G-MELAS subject 242.847
GSM24657A3243G-MELAS subject 359.949
GSM24658A3243G-MELAS subject 432.746
GSM24659A3243G-PEO subject 133.347
GSM24660A3243G-PEO subject 255.658
GSM24661A3243G-PEO subject 351.162
GSM24662A3243G-PEO subject 432.747
GSM24663mtDNA "Common"-deletion subject 176.562
GSM24664mtDNA "Common"-deletion subject 292.754
GSM24665mtDNA "Common"-deletion subject 364.650
GSM24666mtDNA "Common"-deletion subject 443.640