ProfileGDS1065 / 217491_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 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15406.599
GSM24653Normal subject 25566.799
GSM24654Normal subject 35622.199
GSM24655A3243G-MELAS subject 12415.999
GSM24656A3243G-MELAS subject 2379399
GSM24657A3243G-MELAS subject 36970.799
GSM24658A3243G-MELAS subject 44646.999
GSM24659A3243G-PEO subject 13456.199
GSM24660A3243G-PEO subject 23621.199
GSM24661A3243G-PEO subject 33384.599
GSM24662A3243G-PEO subject 44936.499
GSM24663mtDNA "Common"-deletion subject 16234.499
GSM24664mtDNA "Common"-deletion subject 26626.699
GSM24665mtDNA "Common"-deletion subject 36372.899
GSM24666mtDNA "Common"-deletion subject 47641.699