ProfileGDS1065 / 215375_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 52% 44% 53% 53% 58% 43% 52% 52% 51% 65% 54% 56% 45% 53% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 147.952
GSM24653Normal subject 233.344
GSM24654Normal subject 359.253
GSM24655A3243G-MELAS subject 136.253
GSM24656A3243G-MELAS subject 264.758
GSM24657A3243G-MELAS subject 347.443
GSM24658A3243G-MELAS subject 44352
GSM24659A3243G-PEO subject 140.452
GSM24660A3243G-PEO subject 243.551
GSM24661A3243G-PEO subject 357.165
GSM24662A3243G-PEO subject 444.854
GSM24663mtDNA "Common"-deletion subject 158.756
GSM24664mtDNA "Common"-deletion subject 264.645
GSM24665mtDNA "Common"-deletion subject 37453
GSM24666mtDNA "Common"-deletion subject 476.553