ProfileGDS1065 / 219091_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 67% 68% 69% 78% 73% 70% 73% 70% 70% 73% 74% 72% 78% 73% 74% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 190.967
GSM24653Normal subject 287.568
GSM24654Normal subject 3122.569
GSM24655A3243G-MELAS subject 1101.678
GSM24656A3243G-MELAS subject 2119.773
GSM24657A3243G-MELAS subject 3158.570
GSM24658A3243G-MELAS subject 4116.173
GSM24659A3243G-PEO subject 180.470
GSM24660A3243G-PEO subject 293.470
GSM24661A3243G-PEO subject 382.173
GSM24662A3243G-PEO subject 410674
GSM24663mtDNA "Common"-deletion subject 1119.172
GSM24664mtDNA "Common"-deletion subject 2285.878
GSM24665mtDNA "Common"-deletion subject 3178.773
GSM24666mtDNA "Common"-deletion subject 4217.974