ProfileGDS1065 / 221760_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 68% 71% 73% 76% 67% 69% 69% 63% 55% 52% 59% 66% 73% 73% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 194.968
GSM24653Normal subject 2105.871
GSM24654Normal subject 3151.873
GSM24655A3243G-MELAS subject 192.676
GSM24656A3243G-MELAS subject 292.167
GSM24657A3243G-MELAS subject 3157.169
GSM24658A3243G-MELAS subject 493.469
GSM24659A3243G-PEO subject 159.963
GSM24660A3243G-PEO subject 250.755
GSM24661A3243G-PEO subject 334.752
GSM24662A3243G-PEO subject 454.759
GSM24663mtDNA "Common"-deletion subject 189.466
GSM24664mtDNA "Common"-deletion subject 2221.173
GSM24665mtDNA "Common"-deletion subject 3179.573
GSM24666mtDNA "Common"-deletion subject 4276.878