ProfileGDS1065 / 212095_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 45% 45% 69% 19% 57% 43% 61% 47% 48% 42% 33% 53% 53% 52% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 135.645
GSM24653Normal subject 234.345
GSM24654Normal subject 3124.269
GSM24655A3243G-MELAS subject 16.819
GSM24656A3243G-MELAS subject 262.257
GSM24657A3243G-MELAS subject 347.643
GSM24658A3243G-MELAS subject 463.461
GSM24659A3243G-PEO subject 133.847
GSM24660A3243G-PEO subject 238.848
GSM24661A3243G-PEO subject 321.942
GSM24662A3243G-PEO subject 418.133
GSM24663mtDNA "Common"-deletion subject 152.453
GSM24664mtDNA "Common"-deletion subject 286.953
GSM24665mtDNA "Common"-deletion subject 371.552
GSM24666mtDNA "Common"-deletion subject 461.548