ProfileGDS1065 / 213026_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 56% 46% 66% 46% 53% 56% 58% 46% 47% 45% 26% 52% 58% 66% 66% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15856
GSM24653Normal subject 236.646
GSM24654Normal subject 3107.166
GSM24655A3243G-MELAS subject 127.746
GSM24656A3243G-MELAS subject 253.653
GSM24657A3243G-MELAS subject 382.256
GSM24658A3243G-MELAS subject 454.958
GSM24659A3243G-PEO subject 131.946
GSM24660A3243G-PEO subject 23747
GSM24661A3243G-PEO subject 325.345
GSM24662A3243G-PEO subject 41226
GSM24663mtDNA "Common"-deletion subject 149.452
GSM24664mtDNA "Common"-deletion subject 2106.958
GSM24665mtDNA "Common"-deletion subject 3127.666
GSM24666mtDNA "Common"-deletion subject 4143.666