ProfileGDS1065 / 212343_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 77% 75% 79% 61% 67% 69% 72% 67% 79% 75% 75% 74% 82% 73% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1155.777
GSM24653Normal subject 2123.775
GSM24654Normal subject 3219.779
GSM24655A3243G-MELAS subject 147.861
GSM24656A3243G-MELAS subject 29367
GSM24657A3243G-MELAS subject 3152.269
GSM24658A3243G-MELAS subject 4107.572
GSM24659A3243G-PEO subject 171.567
GSM24660A3243G-PEO subject 214779
GSM24661A3243G-PEO subject 39075
GSM24662A3243G-PEO subject 4111.575
GSM24663mtDNA "Common"-deletion subject 1131.674
GSM24664mtDNA "Common"-deletion subject 2357.282
GSM24665mtDNA "Common"-deletion subject 3186.673
GSM24666mtDNA "Common"-deletion subject 4280.978