ProfileGDS1065 / 214744_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 69% 66% 62% 68% 62% 60% 58% 57% 60% 67% 70% 69% 58% 66% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1102.169
GSM24653Normal subject 282.466
GSM24654Normal subject 391.262
GSM24655A3243G-MELAS subject 164.668
GSM24656A3243G-MELAS subject 274.662
GSM24657A3243G-MELAS subject 3100.360
GSM24658A3243G-MELAS subject 455.558
GSM24659A3243G-PEO subject 148.257
GSM24660A3243G-PEO subject 26060
GSM24661A3243G-PEO subject 362.167
GSM24662A3243G-PEO subject 484.470
GSM24663mtDNA "Common"-deletion subject 1101.269
GSM24664mtDNA "Common"-deletion subject 2107.858
GSM24665mtDNA "Common"-deletion subject 3127.466
GSM24666mtDNA "Common"-deletion subject 489.457