ProfileGDS1065 / 206736_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 50% 19% 40% 42% 37% 42% 40% 53% 23% 46% 33% 54% 34% 41% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 144.850
GSM24653Normal subject 27.919
GSM24654Normal subject 334.240
GSM24655A3243G-MELAS subject 12442
GSM24656A3243G-MELAS subject 227.237
GSM24657A3243G-MELAS subject 34542
GSM24658A3243G-MELAS subject 425.840
GSM24659A3243G-PEO subject 142.453
GSM24660A3243G-PEO subject 210.923
GSM24661A3243G-PEO subject 326.246
GSM24662A3243G-PEO subject 417.633
GSM24663mtDNA "Common"-deletion subject 153.754
GSM24664mtDNA "Common"-deletion subject 239.334
GSM24665mtDNA "Common"-deletion subject 343.741
GSM24666mtDNA "Common"-deletion subject 439.738