ProfileGDS1065 / 209448_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 73% 79% 74% 80% 73% 83% 72% 78% 79% 75% 82% 79% 76% 66% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1125.573
GSM24653Normal subject 2160.579
GSM24654Normal subject 3162.574
GSM24655A3243G-MELAS subject 1113.680
GSM24656A3243G-MELAS subject 2119.373
GSM24657A3243G-MELAS subject 3361.983
GSM24658A3243G-MELAS subject 4109.372
GSM24659A3243G-PEO subject 1116.778
GSM24660A3243G-PEO subject 214879
GSM24661A3243G-PEO subject 394.375
GSM24662A3243G-PEO subject 4170.982
GSM24663mtDNA "Common"-deletion subject 1178.179
GSM24664mtDNA "Common"-deletion subject 225976
GSM24665mtDNA "Common"-deletion subject 3131.666
GSM24666mtDNA "Common"-deletion subject 4272.878