ProfileGDS1065 / 202204_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 83% 77% 82% 82% 83% 82% 77% 87% 84% 84% 83% 84% 83% 84% 80% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1229.883
GSM24653Normal subject 2143.377
GSM24654Normal subject 3263.682
GSM24655A3243G-MELAS subject 1126.882
GSM24656A3243G-MELAS subject 222383
GSM24657A3243G-MELAS subject 333982
GSM24658A3243G-MELAS subject 4146.677
GSM24659A3243G-PEO subject 1209.487
GSM24660A3243G-PEO subject 2206.984
GSM24661A3243G-PEO subject 3156.784
GSM24662A3243G-PEO subject 4177.683
GSM24663mtDNA "Common"-deletion subject 1247.884
GSM24664mtDNA "Common"-deletion subject 2396.683
GSM24665mtDNA "Common"-deletion subject 3388.784
GSM24666mtDNA "Common"-deletion subject 4311.980