ProfileGDS1065 / 215167_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 78% 78% 73% 77% 82% 82% 77% 75% 79% 85% 82% 80% 81% 80% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1162.378
GSM24653Normal subject 215478
GSM24654Normal subject 3154.873
GSM24655A3243G-MELAS subject 193.777
GSM24656A3243G-MELAS subject 2204.582
GSM24657A3243G-MELAS subject 3319.982
GSM24658A3243G-MELAS subject 4140.777
GSM24659A3243G-PEO subject 19875
GSM24660A3243G-PEO subject 2145.779
GSM24661A3243G-PEO subject 3169.985
GSM24662A3243G-PEO subject 4164.882
GSM24663mtDNA "Common"-deletion subject 1193.280
GSM24664mtDNA "Common"-deletion subject 2330.981
GSM24665mtDNA "Common"-deletion subject 3273.180
GSM24666mtDNA "Common"-deletion subject 429479