ProfileGDS1065 / 220966_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 94% 94% 93% 93% 91% 93% 94% 94% 94% 95% 95% 96% 92% 92% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1844.994
GSM24653Normal subject 2708.694
GSM24654Normal subject 3870.593
GSM24655A3243G-MELAS subject 1350.393
GSM24656A3243G-MELAS subject 2472.191
GSM24657A3243G-MELAS subject 31031.293
GSM24658A3243G-MELAS subject 4702.594
GSM24659A3243G-PEO subject 1518.894
GSM24660A3243G-PEO subject 2612.894
GSM24661A3243G-PEO subject 3593.495
GSM24662A3243G-PEO subject 482895
GSM24663mtDNA "Common"-deletion subject 11354.896
GSM24664mtDNA "Common"-deletion subject 2869.592
GSM24665mtDNA "Common"-deletion subject 3934.692
GSM24666mtDNA "Common"-deletion subject 4934.292