ProfileGDS1065 / 218036_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 25% 37% 66% 28% 47% 26% 39% 21% 35% 29% 29% 38% 49% 58% 47% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.425
GSM24653Normal subject 224.337
GSM24654Normal subject 3107.666
GSM24655A3243G-MELAS subject 111.928
GSM24656A3243G-MELAS subject 242.247
GSM24657A3243G-MELAS subject 319.126
GSM24658A3243G-MELAS subject 424.839
GSM24659A3243G-PEO subject 19.221
GSM24660A3243G-PEO subject 221.335
GSM24661A3243G-PEO subject 311.429
GSM24662A3243G-PEO subject 413.929
GSM24663mtDNA "Common"-deletion subject 126.238
GSM24664mtDNA "Common"-deletion subject 277.349
GSM24665mtDNA "Common"-deletion subject 392.558
GSM24666mtDNA "Common"-deletion subject 459.147