ProfileGDS1065 / 203518_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 50% 48% 60% 40% 46% 48% 50% 33% 35% 42% 31% 32% 60% 48% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14550
GSM24653Normal subject 239.248
GSM24654Normal subject 381.960
GSM24655A3243G-MELAS subject 122.340
GSM24656A3243G-MELAS subject 240.846
GSM24657A3243G-MELAS subject 359.448
GSM24658A3243G-MELAS subject 439.350
GSM24659A3243G-PEO subject 118.433
GSM24660A3243G-PEO subject 222.235
GSM24661A3243G-PEO subject 322.642
GSM24662A3243G-PEO subject 41631
GSM24663mtDNA "Common"-deletion subject 118.832
GSM24664mtDNA "Common"-deletion subject 2118.760
GSM24665mtDNA "Common"-deletion subject 359.848
GSM24666mtDNA "Common"-deletion subject 475.653