ProfileGDS1065 / 218996_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 70% 65% 55% 62% 61% 74% 56% 73% 66% 73% 72% 72% 54% 62% 66% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1102.670
GSM24653Normal subject 278.965
GSM24654Normal subject 367.155
GSM24655A3243G-MELAS subject 149.262
GSM24656A3243G-MELAS subject 272.361
GSM24657A3243G-MELAS subject 3203.474
GSM24658A3243G-MELAS subject 450.456
GSM24659A3243G-PEO subject 192.573
GSM24660A3243G-PEO subject 276.466
GSM24661A3243G-PEO subject 381.273
GSM24662A3243G-PEO subject 493.672
GSM24663mtDNA "Common"-deletion subject 1121.572
GSM24664mtDNA "Common"-deletion subject 29354
GSM24665mtDNA "Common"-deletion subject 3108.462
GSM24666mtDNA "Common"-deletion subject 4139.266