ProfileGDS1065 / 206319_s_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 37% 18% 33% 40% 39% 35% 42% 39% 44% 21% 30% 33% 42% 39% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 124.837
GSM24653Normal subject 27.318
GSM24654Normal subject 323.233
GSM24655A3243G-MELAS subject 122.240
GSM24656A3243G-MELAS subject 229.739
GSM24657A3243G-MELAS subject 332.535
GSM24658A3243G-MELAS subject 427.742
GSM24659A3243G-PEO subject 124.539
GSM24660A3243G-PEO subject 232.144
GSM24661A3243G-PEO subject 36.721
GSM24662A3243G-PEO subject 414.730
GSM24663mtDNA "Common"-deletion subject 120.333
GSM24664mtDNA "Common"-deletion subject 256.442
GSM24665mtDNA "Common"-deletion subject 34039
GSM24666mtDNA "Common"-deletion subject 429.933