ProfileGDS1065 / 214278_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 37% 22% 30% 36% 60% 23% 47% 59% 23% 54% 21% 24% 39% 42% 40% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 125.437
GSM24653Normal subject 210.122
GSM24654Normal subject 320.130
GSM24655A3243G-MELAS subject 11836
GSM24656A3243G-MELAS subject 269.460
GSM24657A3243G-MELAS subject 314.623
GSM24658A3243G-MELAS subject 434.647
GSM24659A3243G-PEO subject 15359
GSM24660A3243G-PEO subject 21123
GSM24661A3243G-PEO subject 337.354
GSM24662A3243G-PEO subject 48.121
GSM24663mtDNA "Common"-deletion subject 111.424
GSM24664mtDNA "Common"-deletion subject 250.139
GSM24665mtDNA "Common"-deletion subject 345.442
GSM24666mtDNA "Common"-deletion subject 443.740