ProfileGDS1065 / 216311_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 17% 19% 19% 16% 5% 10% 7% 17% 21% 16% 26% 22% 18% 15% 15% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.417
GSM24653Normal subject 27.919
GSM24654Normal subject 39.319
GSM24655A3243G-MELAS subject 15.716
GSM24656A3243G-MELAS subject 23.25
GSM24657A3243G-MELAS subject 35.410
GSM24658A3243G-MELAS subject 42.67
GSM24659A3243G-PEO subject 17.217
GSM24660A3243G-PEO subject 29.321
GSM24661A3243G-PEO subject 3516
GSM24662A3243G-PEO subject 411.426
GSM24663mtDNA "Common"-deletion subject 11022
GSM24664mtDNA "Common"-deletion subject 213.618
GSM24665mtDNA "Common"-deletion subject 38.815
GSM24666mtDNA "Common"-deletion subject 48.415