ProfileGDS1065 / 203817_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 61% 70% 67% 58% 66% 58% 60% 51% 53% 49% 47% 53% 68% 69% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 170.961
GSM24653Normal subject 297.370
GSM24654Normal subject 311167
GSM24655A3243G-MELAS subject 143.458
GSM24656A3243G-MELAS subject 288.266
GSM24657A3243G-MELAS subject 390.458
GSM24658A3243G-MELAS subject 460.660
GSM24659A3243G-PEO subject 13951
GSM24660A3243G-PEO subject 246.253
GSM24661A3243G-PEO subject 330.549
GSM24662A3243G-PEO subject 433.747
GSM24663mtDNA "Common"-deletion subject 151.853
GSM24664mtDNA "Common"-deletion subject 2164.668
GSM24665mtDNA "Common"-deletion subject 3149.469
GSM24666mtDNA "Common"-deletion subject 4149.267