ProfileGDS1065 / 208022_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 3% 9% 23% 29% 2% 25% 31% 35% 3% 8% 9% 9% 6% 14% 24% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123
GSM24653Normal subject 249
GSM24654Normal subject 312.423
GSM24655A3243G-MELAS subject 112.629
GSM24656A3243G-MELAS subject 21.72
GSM24657A3243G-MELAS subject 317.725
GSM24658A3243G-MELAS subject 415.431
GSM24659A3243G-PEO subject 120.735
GSM24660A3243G-PEO subject 21.93
GSM24661A3243G-PEO subject 32.78
GSM24662A3243G-PEO subject 43.29
GSM24663mtDNA "Common"-deletion subject 13.89
GSM24664mtDNA "Common"-deletion subject 25.16
GSM24665mtDNA "Common"-deletion subject 38.214
GSM24666mtDNA "Common"-deletion subject 416.724