ProfileGDS1065 / 211185_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 94% 94% 96% 95% 96% 94% 95% 94% 94% 93% 91% 94% 95% 96% 96% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1781.794
GSM24653Normal subject 2667.694
GSM24654Normal subject 31433.796
GSM24655A3243G-MELAS subject 1505.195
GSM24656A3243G-MELAS subject 21048.196
GSM24657A3243G-MELAS subject 31116.994
GSM24658A3243G-MELAS subject 4858.795
GSM24659A3243G-PEO subject 1466.494
GSM24660A3243G-PEO subject 2587.194
GSM24661A3243G-PEO subject 3411.493
GSM24662A3243G-PEO subject 4385.591
GSM24663mtDNA "Common"-deletion subject 1780.594
GSM24664mtDNA "Common"-deletion subject 21540.695
GSM24665mtDNA "Common"-deletion subject 31666.896
GSM24666mtDNA "Common"-deletion subject 41872.796