ProfileGDS1065 / 207329_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 11% 30% 25% 45% 28% 10% 7% 9% 45% 11% 12% 15% 13% 11% 8% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.511
GSM24653Normal subject 216.730
GSM24654Normal subject 314.425
GSM24655A3243G-MELAS subject 126.845
GSM24656A3243G-MELAS subject 217.628
GSM24657A3243G-MELAS subject 35.410
GSM24658A3243G-MELAS subject 42.67
GSM24659A3243G-PEO subject 13.99
GSM24660A3243G-PEO subject 234.145
GSM24661A3243G-PEO subject 33.611
GSM24662A3243G-PEO subject 44.212
GSM24663mtDNA "Common"-deletion subject 16.315
GSM24664mtDNA "Common"-deletion subject 29.613
GSM24665mtDNA "Common"-deletion subject 36.711
GSM24666mtDNA "Common"-deletion subject 44.38