ProfileGDS1065 / 208035_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 62% 55% 46% 62% 62% 61% 49% 73% 61% 66% 60% 68% 61% 63% 50% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 172.762
GSM24653Normal subject 251.155
GSM24654Normal subject 344.646
GSM24655A3243G-MELAS subject 150.662
GSM24656A3243G-MELAS subject 276.162
GSM24657A3243G-MELAS subject 3107.161
GSM24658A3243G-MELAS subject 437.149
GSM24659A3243G-PEO subject 190.173
GSM24660A3243G-PEO subject 264.261
GSM24661A3243G-PEO subject 360.466
GSM24662A3243G-PEO subject 455.760
GSM24663mtDNA "Common"-deletion subject 1100.168
GSM24664mtDNA "Common"-deletion subject 2121.461
GSM24665mtDNA "Common"-deletion subject 3112.263
GSM24666mtDNA "Common"-deletion subject 46650