ProfileGDS1065 / 214081_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 66% 62% 60% 60% 60% 61% 65% 71% 58% 67% 67% 67% 59% 60% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18866
GSM24653Normal subject 268.162
GSM24654Normal subject 383.660
GSM24655A3243G-MELAS subject 147.260
GSM24656A3243G-MELAS subject 269.160
GSM24657A3243G-MELAS subject 3105.661
GSM24658A3243G-MELAS subject 476.765
GSM24659A3243G-PEO subject 182.971
GSM24660A3243G-PEO subject 256.258
GSM24661A3243G-PEO subject 364.567
GSM24662A3243G-PEO subject 473.167
GSM24663mtDNA "Common"-deletion subject 194.267
GSM24664mtDNA "Common"-deletion subject 2115.959
GSM24665mtDNA "Common"-deletion subject 39860
GSM24666mtDNA "Common"-deletion subject 4112.362