ProfileGDS1065 / 211695_x_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 48% 44% 42% 38% 50% 42% 39% 57% 50% 54% 56% 49% 47% 52% 45% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 141.648
GSM24653Normal subject 232.844
GSM24654Normal subject 336.342
GSM24655A3243G-MELAS subject 120.338
GSM24656A3243G-MELAS subject 247.850
GSM24657A3243G-MELAS subject 344.242
GSM24658A3243G-MELAS subject 424.239
GSM24659A3243G-PEO subject 148.857
GSM24660A3243G-PEO subject 241.250
GSM24661A3243G-PEO subject 336.854
GSM24662A3243G-PEO subject 447.456
GSM24663mtDNA "Common"-deletion subject 144.649
GSM24664mtDNA "Common"-deletion subject 271.147
GSM24665mtDNA "Common"-deletion subject 372.352
GSM24666mtDNA "Common"-deletion subject 453.645