ProfileGDS1065 / 220007_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 50% 43% 41% 27% 42% 47% 42% 37% 41% 50% 49% 39% 33% 49% 46% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 144.550
GSM24653Normal subject 231.443
GSM24654Normal subject 33541
GSM24655A3243G-MELAS subject 111.227
GSM24656A3243G-MELAS subject 234.942
GSM24657A3243G-MELAS subject 355.747
GSM24658A3243G-MELAS subject 427.742
GSM24659A3243G-PEO subject 122.237
GSM24660A3243G-PEO subject 228.341
GSM24661A3243G-PEO subject 331.950
GSM24662A3243G-PEO subject 436.249
GSM24663mtDNA "Common"-deletion subject 128.239
GSM24664mtDNA "Common"-deletion subject 236.833
GSM24665mtDNA "Common"-deletion subject 363.149
GSM24666mtDNA "Common"-deletion subject 45646