ProfileGDS1065 / 203316_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 93% 95% 93% 95% 94% 94% 93% 95% 94% 94% 94% 94% 95% 93% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 160493
GSM24653Normal subject 2818.295
GSM24654Normal subject 3760.993
GSM24655A3243G-MELAS subject 1519.795
GSM24656A3243G-MELAS subject 271494
GSM24657A3243G-MELAS subject 31171.494
GSM24658A3243G-MELAS subject 4548.693
GSM24659A3243G-PEO subject 153995
GSM24660A3243G-PEO subject 2678.194
GSM24661A3243G-PEO subject 3493.594
GSM24662A3243G-PEO subject 4603.794
GSM24663mtDNA "Common"-deletion subject 1788.994
GSM24664mtDNA "Common"-deletion subject 21405.995
GSM24665mtDNA "Common"-deletion subject 31103.193
GSM24666mtDNA "Common"-deletion subject 41617.395