ProfileGDS1065 / 214888_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 54% 59% 34% 61% 61% 47% 44% 71% 61% 62% 61% 66% 53% 46% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 153.254
GSM24653Normal subject 259.759
GSM24654Normal subject 325.534
GSM24655A3243G-MELAS subject 148.861
GSM24656A3243G-MELAS subject 27161
GSM24657A3243G-MELAS subject 355.547
GSM24658A3243G-MELAS subject 430.744
GSM24659A3243G-PEO subject 182.671
GSM24660A3243G-PEO subject 264.461
GSM24661A3243G-PEO subject 35062
GSM24662A3243G-PEO subject 459.161
GSM24663mtDNA "Common"-deletion subject 187.666
GSM24664mtDNA "Common"-deletion subject 289.153
GSM24665mtDNA "Common"-deletion subject 354.346
GSM24666mtDNA "Common"-deletion subject 448.743