ProfileGDS1065 / 212128_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 49% 54% 63% 50% 60% 54% 49% 67% 56% 53% 41% 54% 54% 60% 55% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 142.849
GSM24653Normal subject 250.954
GSM24654Normal subject 392.563
GSM24655A3243G-MELAS subject 132.550
GSM24656A3243G-MELAS subject 270.260
GSM24657A3243G-MELAS subject 377.854
GSM24658A3243G-MELAS subject 437.649
GSM24659A3243G-PEO subject 169.567
GSM24660A3243G-PEO subject 253.156
GSM24661A3243G-PEO subject 335.553
GSM24662A3243G-PEO subject 425.841
GSM24663mtDNA "Common"-deletion subject 153.454
GSM24664mtDNA "Common"-deletion subject 293.654
GSM24665mtDNA "Common"-deletion subject 39860
GSM24666mtDNA "Common"-deletion subject 483.555