ProfileGDS1065 / 204990_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 15% 50% 52% 55% 14% 32% 45% 20% 19% 59% 47% 43% 8% 32% 44% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.315
GSM24653Normal subject 242.150
GSM24654Normal subject 358.952
GSM24655A3243G-MELAS subject 138.955
GSM24656A3243G-MELAS subject 26.514
GSM24657A3243G-MELAS subject 326.832
GSM24658A3243G-MELAS subject 431.245
GSM24659A3243G-PEO subject 18.720
GSM24660A3243G-PEO subject 28.319
GSM24661A3243G-PEO subject 344.959
GSM24662A3243G-PEO subject 433.447
GSM24663mtDNA "Common"-deletion subject 132.943
GSM24664mtDNA "Common"-deletion subject 268
GSM24665mtDNA "Common"-deletion subject 328.432
GSM24666mtDNA "Common"-deletion subject 450.344