ProfileGDS1065 / 215281_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 35% 1% 45% 14% 25% 20% 36% 31% 34% 15% 53% 36% 34% 22% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 122.635
GSM24653Normal subject 21.31
GSM24654Normal subject 341.845
GSM24655A3243G-MELAS subject 1514
GSM24656A3243G-MELAS subject 21425
GSM24657A3243G-MELAS subject 312.220
GSM24658A3243G-MELAS subject 421.136
GSM24659A3243G-PEO subject 116.331
GSM24660A3243G-PEO subject 22134
GSM24661A3243G-PEO subject 34.715
GSM24662A3243G-PEO subject 44253
GSM24663mtDNA "Common"-deletion subject 123.236
GSM24664mtDNA "Common"-deletion subject 239.634
GSM24665mtDNA "Common"-deletion subject 314.922
GSM24666mtDNA "Common"-deletion subject 426.431