ProfileGDS1065 / 205410_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 44% 59% 42% 48% 57% 39% 43% 52% 41% 29% 49% 40% 42% 43% 34% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 135.344
GSM24653Normal subject 259.959
GSM24654Normal subject 337.842
GSM24655A3243G-MELAS subject 129.848
GSM24656A3243G-MELAS subject 261.157
GSM24657A3243G-MELAS subject 338.539
GSM24658A3243G-MELAS subject 429.343
GSM24659A3243G-PEO subject 14052
GSM24660A3243G-PEO subject 228.841
GSM24661A3243G-PEO subject 311.529
GSM24662A3243G-PEO subject 436.349
GSM24663mtDNA "Common"-deletion subject 129.640
GSM24664mtDNA "Common"-deletion subject 257.142
GSM24665mtDNA "Common"-deletion subject 349.243
GSM24666mtDNA "Common"-deletion subject 430.934