ProfileGDS1065 / 215479_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 59% 63% 58% 66% 63% 57% 54% 65% 61% 56% 57% 65% 65% 61% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 164.759
GSM24653Normal subject 27263
GSM24654Normal subject 373.658
GSM24655A3243G-MELAS subject 158.766
GSM24656A3243G-MELAS subject 277.463
GSM24657A3243G-MELAS subject 385.757
GSM24658A3243G-MELAS subject 446.754
GSM24659A3243G-PEO subject 166.365
GSM24660A3243G-PEO subject 263.461
GSM24661A3243G-PEO subject 340.856
GSM24662A3243G-PEO subject 449.457
GSM24663mtDNA "Common"-deletion subject 184.165
GSM24664mtDNA "Common"-deletion subject 2145.465
GSM24665mtDNA "Common"-deletion subject 3102.261
GSM24666mtDNA "Common"-deletion subject 484.656