ProfileGDS1065 / 208899_x_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 79% 76% 91% 86% 82% 80% 83% 73% 80% 75% 76% 80% 83% 88% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 117179
GSM24653Normal subject 2134.776
GSM24654Normal subject 3577.491
GSM24655A3243G-MELAS subject 1170.286
GSM24656A3243G-MELAS subject 2203.782
GSM24657A3243G-MELAS subject 3279.580
GSM24658A3243G-MELAS subject 4207.383
GSM24659A3243G-PEO subject 188.973
GSM24660A3243G-PEO subject 2152.180
GSM24661A3243G-PEO subject 392.275
GSM24662A3243G-PEO subject 4116.976
GSM24663mtDNA "Common"-deletion subject 1193.980
GSM24664mtDNA "Common"-deletion subject 2397.583
GSM24665mtDNA "Common"-deletion subject 3544.888
GSM24666mtDNA "Common"-deletion subject 4397.683