ProfileGDS1065 / 209646_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 38% 46% 42% 51% 48% 56% 50% 55% 43% 54% 43% 51% 51% 45% 46% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 127.138
GSM24653Normal subject 236.346
GSM24654Normal subject 337.742
GSM24655A3243G-MELAS subject 133.251
GSM24656A3243G-MELAS subject 243.548
GSM24657A3243G-MELAS subject 383.756
GSM24658A3243G-MELAS subject 438.850
GSM24659A3243G-PEO subject 145.155
GSM24660A3243G-PEO subject 231.143
GSM24661A3243G-PEO subject 337.454
GSM24662A3243G-PEO subject 428.343
GSM24663mtDNA "Common"-deletion subject 147.651
GSM24664mtDNA "Common"-deletion subject 282.151
GSM24665mtDNA "Common"-deletion subject 352.645
GSM24666mtDNA "Common"-deletion subject 455.646