ProfileGDS1065 / 208037_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 66% 56% 61% 64% 59% 52% 61% 74% 68% 76% 64% 68% 58% 59% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 185.866
GSM24653Normal subject 253.256
GSM24654Normal subject 38661
GSM24655A3243G-MELAS subject 155.164
GSM24656A3243G-MELAS subject 266.259
GSM24657A3243G-MELAS subject 371.352
GSM24658A3243G-MELAS subject 463.361
GSM24659A3243G-PEO subject 196.974
GSM24660A3243G-PEO subject 284.168
GSM24661A3243G-PEO subject 395.776
GSM24662A3243G-PEO subject 465.764
GSM24663mtDNA "Common"-deletion subject 1100.868
GSM24664mtDNA "Common"-deletion subject 2109.558
GSM24665mtDNA "Common"-deletion subject 396.659
GSM24666mtDNA "Common"-deletion subject 487.356