ProfileGDS1065 / 220451_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 44% 43% 43% 49% 47% 47% 39% 48% 52% 48% 49% 48% 40% 43% 36% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 135.244
GSM24653Normal subject 232.243
GSM24654Normal subject 339.643
GSM24655A3243G-MELAS subject 130.849
GSM24656A3243G-MELAS subject 242.447
GSM24657A3243G-MELAS subject 356.747
GSM24658A3243G-MELAS subject 424.339
GSM24659A3243G-PEO subject 134.548
GSM24660A3243G-PEO subject 245.252
GSM24661A3243G-PEO subject 328.748
GSM24662A3243G-PEO subject 435.549
GSM24663mtDNA "Common"-deletion subject 141.148
GSM24664mtDNA "Common"-deletion subject 252.840
GSM24665mtDNA "Common"-deletion subject 348.943
GSM24666mtDNA "Common"-deletion subject 434.336