ProfileGDS1065 / 214509_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% 37% 25% 12% 43% 29% 35% 40% 41% 40% 20% 14% 34% 36% 26% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123.235
GSM24653Normal subject 22437
GSM24654Normal subject 314.325
GSM24655A3243G-MELAS subject 14.312
GSM24656A3243G-MELAS subject 236.243
GSM24657A3243G-MELAS subject 323.329
GSM24658A3243G-MELAS subject 419.735
GSM24659A3243G-PEO subject 125.640
GSM24660A3243G-PEO subject 228.541
GSM24661A3243G-PEO subject 32040
GSM24662A3243G-PEO subject 47.620
GSM24663mtDNA "Common"-deletion subject 15.914
GSM24664mtDNA "Common"-deletion subject 239.234
GSM24665mtDNA "Common"-deletion subject 334.836
GSM24666mtDNA "Common"-deletion subject 419.226