ProfileGDS1065 / 203687_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 57% 64% 55% 39% 62% 38% 55% 33% 57% 66% 53% 57% 60% 58% 37% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 159.857
GSM24653Normal subject 274.964
GSM24654Normal subject 366.155
GSM24655A3243G-MELAS subject 121.439
GSM24656A3243G-MELAS subject 275.862
GSM24657A3243G-MELAS subject 336.438
GSM24658A3243G-MELAS subject 449.555
GSM24659A3243G-PEO subject 118.133
GSM24660A3243G-PEO subject 254.957
GSM24661A3243G-PEO subject 358.966
GSM24662A3243G-PEO subject 443.153
GSM24663mtDNA "Common"-deletion subject 159.757
GSM24664mtDNA "Common"-deletion subject 2118.960
GSM24665mtDNA "Common"-deletion subject 392.258
GSM24666mtDNA "Common"-deletion subject 437.637