ProfileGDS1065 / 201270_x_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 93% 92% 91% 90% 92% 91% 92% 93% 93% 93% 93% 93% 91% 93% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 169293
GSM24653Normal subject 2502.892
GSM24654Normal subject 3598.391
GSM24655A3243G-MELAS subject 1255.290
GSM24656A3243G-MELAS subject 2512.992
GSM24657A3243G-MELAS subject 3761.491
GSM24658A3243G-MELAS subject 4476.792
GSM24659A3243G-PEO subject 1389.793
GSM24660A3243G-PEO subject 2557.593
GSM24661A3243G-PEO subject 3431.493
GSM24662A3243G-PEO subject 4527.193
GSM24663mtDNA "Common"-deletion subject 1685.693
GSM24664mtDNA "Common"-deletion subject 2794.991
GSM24665mtDNA "Common"-deletion subject 3957.493
GSM24666mtDNA "Common"-deletion subject 484491