ProfileGDS1065 / 217792_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 75% 75% 79% 74% 74% 74% 77% 69% 72% 69% 65% 64% 76% 80% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113475
GSM24653Normal subject 2126.575
GSM24654Normal subject 3213.479
GSM24655A3243G-MELAS subject 181.174
GSM24656A3243G-MELAS subject 2127.374
GSM24657A3243G-MELAS subject 320574
GSM24658A3243G-MELAS subject 4146.577
GSM24659A3243G-PEO subject 175.369
GSM24660A3243G-PEO subject 299.772
GSM24661A3243G-PEO subject 369.569
GSM24662A3243G-PEO subject 468.165
GSM24663mtDNA "Common"-deletion subject 182.864
GSM24664mtDNA "Common"-deletion subject 2250.576
GSM24665mtDNA "Common"-deletion subject 3289.480
GSM24666mtDNA "Common"-deletion subject 4198.773