ProfileGDS1065 / 216091_s_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 52% 49% 61% 54% 48% 51% 49% 50% 56% 53% 44% 63% 61% 55% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 147.952
GSM24653Normal subject 240.849
GSM24654Normal subject 385.261
GSM24655A3243G-MELAS subject 137.754
GSM24656A3243G-MELAS subject 24348
GSM24657A3243G-MELAS subject 366.451
GSM24658A3243G-MELAS subject 437.349
GSM24659A3243G-PEO subject 137.250
GSM24660A3243G-PEO subject 252.256
GSM24661A3243G-PEO subject 335.953
GSM24662A3243G-PEO subject 42944
GSM24663mtDNA "Common"-deletion subject 177.463
GSM24664mtDNA "Common"-deletion subject 2122.261
GSM24665mtDNA "Common"-deletion subject 381.455
GSM24666mtDNA "Common"-deletion subject 474.253