ProfileGDS1065 / 209126_x_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 40% 22% 28% 24% 50% 33% 22% 36% 57% 38% 47% 34% 50% 50% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 129.440
GSM24653Normal subject 21022
GSM24654Normal subject 316.828
GSM24655A3243G-MELAS subject 19.124
GSM24656A3243G-MELAS subject 246.950
GSM24657A3243G-MELAS subject 328.333
GSM24658A3243G-MELAS subject 4922
GSM24659A3243G-PEO subject 121.236
GSM24660A3243G-PEO subject 25457
GSM24661A3243G-PEO subject 318.838
GSM24662A3243G-PEO subject 432.747
GSM24663mtDNA "Common"-deletion subject 121.634
GSM24664mtDNA "Common"-deletion subject 278.350
GSM24665mtDNA "Common"-deletion subject 363.950
GSM24666mtDNA "Common"-deletion subject 429.533