ProfileGDS1065 / 209084_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 37% 26% 54% 37% 39% 39% 40% 12% 32% 34% 36% 35% 55% 45% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 124.837
GSM24653Normal subject 21326
GSM24654Normal subject 362.754
GSM24655A3243G-MELAS subject 118.937
GSM24656A3243G-MELAS subject 229.939
GSM24657A3243G-MELAS subject 338.339
GSM24658A3243G-MELAS subject 425.440
GSM24659A3243G-PEO subject 14.912
GSM24660A3243G-PEO subject 218.732
GSM24661A3243G-PEO subject 315.234
GSM24662A3243G-PEO subject 420.836
GSM24663mtDNA "Common"-deletion subject 123.135
GSM24664mtDNA "Common"-deletion subject 294.255
GSM24665mtDNA "Common"-deletion subject 353.145
GSM24666mtDNA "Common"-deletion subject 472.852