ProfileGDS1065 / 220804_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 18% 13% 25% 15% 16% 20% 19% 42% 16% 14% 21% 22% 16% 15% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.618
GSM24653Normal subject 25.213
GSM24654Normal subject 314.125
GSM24655A3243G-MELAS subject 15.315
GSM24656A3243G-MELAS subject 27.516
GSM24657A3243G-MELAS subject 311.920
GSM24658A3243G-MELAS subject 46.819
GSM24659A3243G-PEO subject 127.542
GSM24660A3243G-PEO subject 26.716
GSM24661A3243G-PEO subject 34.214
GSM24662A3243G-PEO subject 48.421
GSM24663mtDNA "Common"-deletion subject 110.122
GSM24664mtDNA "Common"-deletion subject 212.116
GSM24665mtDNA "Common"-deletion subject 38.715
GSM24666mtDNA "Common"-deletion subject 4814