ProfileGDS1065 / 210685_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 42% 34% 60% 38% 46% 50% 56% 42% 50% 36% 43% 45% 43% 55% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132.342
GSM24653Normal subject 221.734
GSM24654Normal subject 383.760
GSM24655A3243G-MELAS subject 119.838
GSM24656A3243G-MELAS subject 240.646
GSM24657A3243G-MELAS subject 365.250
GSM24658A3243G-MELAS subject 449.756
GSM24659A3243G-PEO subject 127.442
GSM24660A3243G-PEO subject 241.350
GSM24661A3243G-PEO subject 316.536
GSM24662A3243G-PEO subject 428.543
GSM24663mtDNA "Common"-deletion subject 137.645
GSM24664mtDNA "Common"-deletion subject 260.343
GSM24665mtDNA "Common"-deletion subject 381.455
GSM24666mtDNA "Common"-deletion subject 488.557