ProfileGDS1065 / 220865_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 63% 65% 70% 74% 67% 62% 65% 60% 67% 64% 72% 70% 68% 68% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 176.263
GSM24653Normal subject 279.865
GSM24654Normal subject 3132.870
GSM24655A3243G-MELAS subject 182.974
GSM24656A3243G-MELAS subject 292.867
GSM24657A3243G-MELAS subject 3108.662
GSM24658A3243G-MELAS subject 474.965
GSM24659A3243G-PEO subject 154.760
GSM24660A3243G-PEO subject 28167
GSM24661A3243G-PEO subject 354.764
GSM24662A3243G-PEO subject 493.772
GSM24663mtDNA "Common"-deletion subject 1108.270
GSM24664mtDNA "Common"-deletion subject 2172.268
GSM24665mtDNA "Common"-deletion subject 3144.868
GSM24666mtDNA "Common"-deletion subject 4150.767