ProfileGDS1065 / 208090_s_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 36% 34% 31% 23% 45% 26% 24% 24% 20% 33% 28% 23% 18% 20% 19% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 124.136
GSM24653Normal subject 22134
GSM24654Normal subject 320.431
GSM24655A3243G-MELAS subject 1923
GSM24656A3243G-MELAS subject 238.345
GSM24657A3243G-MELAS subject 31926
GSM24658A3243G-MELAS subject 41024
GSM24659A3243G-PEO subject 111.324
GSM24660A3243G-PEO subject 2920
GSM24661A3243G-PEO subject 314.133
GSM24662A3243G-PEO subject 41328
GSM24663mtDNA "Common"-deletion subject 110.623
GSM24664mtDNA "Common"-deletion subject 21418
GSM24665mtDNA "Common"-deletion subject 312.520
GSM24666mtDNA "Common"-deletion subject 411.919