ProfileGDS1065 / 213234_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 63% 65% 67% 75% 66% 60% 61% 70% 67% 59% 54% 71% 65% 65% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 177.163
GSM24653Normal subject 277.165
GSM24654Normal subject 3114.167
GSM24655A3243G-MELAS subject 185.175
GSM24656A3243G-MELAS subject 288.166
GSM24657A3243G-MELAS subject 310060
GSM24658A3243G-MELAS subject 463.461
GSM24659A3243G-PEO subject 178.470
GSM24660A3243G-PEO subject 281.467
GSM24661A3243G-PEO subject 34659
GSM24662A3243G-PEO subject 443.554
GSM24663mtDNA "Common"-deletion subject 1113.671
GSM24664mtDNA "Common"-deletion subject 2149.765
GSM24665mtDNA "Common"-deletion subject 3124.265
GSM24666mtDNA "Common"-deletion subject 492.758