ProfileGDS1065 / 215524_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 17% 12% 4% 28% 14% 2% 3% 25% 13% 9% 33% 7% 23% 26% 2% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.117
GSM24653Normal subject 2512
GSM24654Normal subject 32.54
GSM24655A3243G-MELAS subject 112.228
GSM24656A3243G-MELAS subject 26.714
GSM24657A3243G-MELAS subject 32.12
GSM24658A3243G-MELAS subject 41.53
GSM24659A3243G-PEO subject 111.825
GSM24660A3243G-PEO subject 25.313
GSM24661A3243G-PEO subject 339
GSM24662A3243G-PEO subject 418.333
GSM24663mtDNA "Common"-deletion subject 13.47
GSM24664mtDNA "Common"-deletion subject 220.523
GSM24665mtDNA "Common"-deletion subject 320.226
GSM24666mtDNA "Common"-deletion subject 41.92