ProfileGDS1065 / 215461_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 62% 52% 51% 60% 61% 39% 58% 56% 51% 34% 47% 60% 48% 52% 45% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 172.962
GSM24653Normal subject 246.152
GSM24654Normal subject 355.351
GSM24655A3243G-MELAS subject 146.660
GSM24656A3243G-MELAS subject 271.261
GSM24657A3243G-MELAS subject 339.739
GSM24658A3243G-MELAS subject 455.558
GSM24659A3243G-PEO subject 146.856
GSM24660A3243G-PEO subject 243.651
GSM24661A3243G-PEO subject 314.834
GSM24662A3243G-PEO subject 433.747
GSM24663mtDNA "Common"-deletion subject 170.560
GSM24664mtDNA "Common"-deletion subject 273.248
GSM24665mtDNA "Common"-deletion subject 371.552
GSM24666mtDNA "Common"-deletion subject 452.545