ProfileGDS1065 / 203555_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 39% 37% 63% 42% 40% 38% 36% 50% 60% 47% 43% 60% 41% 38% 40% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 127.339
GSM24653Normal subject 224.537
GSM24654Normal subject 392.863
GSM24655A3243G-MELAS subject 124.342
GSM24656A3243G-MELAS subject 23240
GSM24657A3243G-MELAS subject 336.938
GSM24658A3243G-MELAS subject 421.236
GSM24659A3243G-PEO subject 137.150
GSM24660A3243G-PEO subject 261.360
GSM24661A3243G-PEO subject 327.847
GSM24662A3243G-PEO subject 427.743
GSM24663mtDNA "Common"-deletion subject 169.360
GSM24664mtDNA "Common"-deletion subject 253.341
GSM24665mtDNA "Common"-deletion subject 339.338
GSM24666mtDNA "Common"-deletion subject 442.240