ProfileGDS1065 / 203604_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 33% 48% 40% 34% 32% 28% 46% 24% 24% 16% 2% 30% 41% 33% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.433
GSM24653Normal subject 240.148
GSM24654Normal subject 33340
GSM24655A3243G-MELAS subject 116.434
GSM24656A3243G-MELAS subject 22232
GSM24657A3243G-MELAS subject 321.528
GSM24658A3243G-MELAS subject 432.946
GSM24659A3243G-PEO subject 111.324
GSM24660A3243G-PEO subject 211.724
GSM24661A3243G-PEO subject 3516
GSM24662A3243G-PEO subject 41.32
GSM24663mtDNA "Common"-deletion subject 116.830
GSM24664mtDNA "Common"-deletion subject 253.741
GSM24665mtDNA "Common"-deletion subject 330.633
GSM24666mtDNA "Common"-deletion subject 427.331