ProfileGDS1065 / 203344_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% 48% 26% 54% 53% 56% 54% 68% 58% 44% 59% 70% 63% 56% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18666
GSM24653Normal subject 239.348
GSM24654Normal subject 314.926
GSM24655A3243G-MELAS subject 137.654
GSM24656A3243G-MELAS subject 252.253
GSM24657A3243G-MELAS subject 384.156
GSM24658A3243G-MELAS subject 446.554
GSM24659A3243G-PEO subject 17268
GSM24660A3243G-PEO subject 256.158
GSM24661A3243G-PEO subject 324.144
GSM24662A3243G-PEO subject 454.559
GSM24663mtDNA "Common"-deletion subject 1106.470
GSM24664mtDNA "Common"-deletion subject 2132.963
GSM24665mtDNA "Common"-deletion subject 385.556
GSM24666mtDNA "Common"-deletion subject 497.759