ProfileGDS1065 / 214030_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 72% 68% 74% 68% 79% 73% 69% 75% 65% 76% 72% 79% 75% 73% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1118.372
GSM24653Normal subject 288.668
GSM24654Normal subject 3164.274
GSM24655A3243G-MELAS subject 164.368
GSM24656A3243G-MELAS subject 2164.179
GSM24657A3243G-MELAS subject 3193.573
GSM24658A3243G-MELAS subject 491.669
GSM24659A3243G-PEO subject 110275
GSM24660A3243G-PEO subject 273.965
GSM24661A3243G-PEO subject 394.776
GSM24662A3243G-PEO subject 494.972
GSM24663mtDNA "Common"-deletion subject 1176.679
GSM24664mtDNA "Common"-deletion subject 2237.775
GSM24665mtDNA "Common"-deletion subject 3180.173
GSM24666mtDNA "Common"-deletion subject 4199.473