ProfileGDS1065 / 208303_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 20% 21% 28% 20% 25% 22% 20% 23% 23% 23% 20% 52% 15% 16% 19% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.120
GSM24653Normal subject 29.321
GSM24654Normal subject 317.728
GSM24655A3243G-MELAS subject 1720
GSM24656A3243G-MELAS subject 214.625
GSM24657A3243G-MELAS subject 313.422
GSM24658A3243G-MELAS subject 47.620
GSM24659A3243G-PEO subject 110.523
GSM24660A3243G-PEO subject 211.123
GSM24661A3243G-PEO subject 37.523
GSM24662A3243G-PEO subject 47.420
GSM24663mtDNA "Common"-deletion subject 150.252
GSM24664mtDNA "Common"-deletion subject 211.315
GSM24665mtDNA "Common"-deletion subject 39.516
GSM24666mtDNA "Common"-deletion subject 411.519