ProfileGDS1065 / 212618_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 15% 18% 23% 10% 17% 12% 15% 14% 15% 16% 19% 13% 14% 16% 16% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.315
GSM24653Normal subject 27.418
GSM24654Normal subject 312.223
GSM24655A3243G-MELAS subject 13.610
GSM24656A3243G-MELAS subject 28.517
GSM24657A3243G-MELAS subject 36.312
GSM24658A3243G-MELAS subject 44.915
GSM24659A3243G-PEO subject 1614
GSM24660A3243G-PEO subject 26.515
GSM24661A3243G-PEO subject 3516
GSM24662A3243G-PEO subject 4719
GSM24663mtDNA "Common"-deletion subject 15.713
GSM24664mtDNA "Common"-deletion subject 210.214
GSM24665mtDNA "Common"-deletion subject 39.516
GSM24666mtDNA "Common"-deletion subject 49.216