ProfileGDS1065 / 202957_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% 69% 64% 71% 69% 71% 68% 75% 72% 69% 74% 62% 73% 65% 66% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 187.866
GSM24653Normal subject 295.569
GSM24654Normal subject 397.364
GSM24655A3243G-MELAS subject 172.971
GSM24656A3243G-MELAS subject 298.769
GSM24657A3243G-MELAS subject 3172.171
GSM24658A3243G-MELAS subject 486.568
GSM24659A3243G-PEO subject 1100.275
GSM24660A3243G-PEO subject 210072
GSM24661A3243G-PEO subject 368.369
GSM24662A3243G-PEO subject 4102.474
GSM24663mtDNA "Common"-deletion subject 176.362
GSM24664mtDNA "Common"-deletion subject 2210.673
GSM24665mtDNA "Common"-deletion subject 3124.565
GSM24666mtDNA "Common"-deletion subject 4142.566