ProfileGDS1065 / 202796_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% 78% 73% 75% 74% 78% 73% 74% 69% 77% 72% 61% 70% 68% 66% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1136.975
GSM24653Normal subject 2153.178
GSM24654Normal subject 3155.773
GSM24655A3243G-MELAS subject 185.475
GSM24656A3243G-MELAS subject 212474
GSM24657A3243G-MELAS subject 3252.778
GSM24658A3243G-MELAS subject 4110.873
GSM24659A3243G-PEO subject 196.474
GSM24660A3243G-PEO subject 288.269
GSM24661A3243G-PEO subject 3101.977
GSM24662A3243G-PEO subject 495.572
GSM24663mtDNA "Common"-deletion subject 173.361
GSM24664mtDNA "Common"-deletion subject 2187.170
GSM24665mtDNA "Common"-deletion subject 314468
GSM24666mtDNA "Common"-deletion subject 4139.466