ProfileGDS1065 / 213039_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% 73% 73% 74% 70% 81% 77% 75% 72% 82% 76% 77% 73% 76% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1165.678
GSM24653Normal subject 2116.573
GSM24654Normal subject 3152.573
GSM24655A3243G-MELAS subject 184.574
GSM24656A3243G-MELAS subject 2104.170
GSM24657A3243G-MELAS subject 3298.981
GSM24658A3243G-MELAS subject 4143.677
GSM24659A3243G-PEO subject 1102.275
GSM24660A3243G-PEO subject 299.572
GSM24661A3243G-PEO subject 3140.882
GSM24662A3243G-PEO subject 411676
GSM24663mtDNA "Common"-deletion subject 1156.477
GSM24664mtDNA "Common"-deletion subject 2217.973
GSM24665mtDNA "Common"-deletion subject 3215.176
GSM24666mtDNA "Common"-deletion subject 420273