ProfileGDS1065 / 214710_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 42% 35% 41% 42% 47% 36% 34% 46% 45% 39% 44% 52% 43% 38% 46% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 131.742
GSM24653Normal subject 22235
GSM24654Normal subject 335.241
GSM24655A3243G-MELAS subject 124.242
GSM24656A3243G-MELAS subject 241.747
GSM24657A3243G-MELAS subject 333.636
GSM24658A3243G-MELAS subject 41934
GSM24659A3243G-PEO subject 132.346
GSM24660A3243G-PEO subject 23445
GSM24661A3243G-PEO subject 31939
GSM24662A3243G-PEO subject 43044
GSM24663mtDNA "Common"-deletion subject 149.552
GSM24664mtDNA "Common"-deletion subject 259.543
GSM24665mtDNA "Common"-deletion subject 338.238
GSM24666mtDNA "Common"-deletion subject 45646