ProfileGDS1065 / 201689_s_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% 27% 66% 37% 41% 30% 43% 31% 41% 27% 24% 39% 50% 53% 54% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123.335
GSM24653Normal subject 214.327
GSM24654Normal subject 3107.466
GSM24655A3243G-MELAS subject 118.837
GSM24656A3243G-MELAS subject 232.341
GSM24657A3243G-MELAS subject 324.630
GSM24658A3243G-MELAS subject 429.343
GSM24659A3243G-PEO subject 116.831
GSM24660A3243G-PEO subject 228.441
GSM24661A3243G-PEO subject 39.927
GSM24662A3243G-PEO subject 49.924
GSM24663mtDNA "Common"-deletion subject 128.239
GSM24664mtDNA "Common"-deletion subject 279.450
GSM24665mtDNA "Common"-deletion subject 375.353
GSM24666mtDNA "Common"-deletion subject 479.154