ProfileGDS1065 / 207351_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 41% 56% 39% 64% 58% 54% 50% 63% 59% 50% 70% 56% 52% 60% 49% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 130.341
GSM24653Normal subject 253.456
GSM24654Normal subject 331.839
GSM24655A3243G-MELAS subject 15564
GSM24656A3243G-MELAS subject 264.658
GSM24657A3243G-MELAS subject 375.154
GSM24658A3243G-MELAS subject 439.850
GSM24659A3243G-PEO subject 159.863
GSM24660A3243G-PEO subject 259.159
GSM24661A3243G-PEO subject 332.150
GSM24662A3243G-PEO subject 484.770
GSM24663mtDNA "Common"-deletion subject 158.356
GSM24664mtDNA "Common"-deletion subject 284.652
GSM24665mtDNA "Common"-deletion subject 397.360
GSM24666mtDNA "Common"-deletion subject 46349