ProfileGDS1065 / 205193_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 60% 61% 56% 63% 63% 57% 66% 73% 63% 56% 67% 58% 57% 64% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 165.860
GSM24653Normal subject 266.261
GSM24654Normal subject 367.556
GSM24655A3243G-MELAS subject 151.563
GSM24656A3243G-MELAS subject 278.163
GSM24657A3243G-MELAS subject 385.657
GSM24658A3243G-MELAS subject 479.966
GSM24659A3243G-PEO subject 190.673
GSM24660A3243G-PEO subject 268.963
GSM24661A3243G-PEO subject 340.256
GSM24662A3243G-PEO subject 474.267
GSM24663mtDNA "Common"-deletion subject 164.258
GSM24664mtDNA "Common"-deletion subject 2104.757
GSM24665mtDNA "Common"-deletion subject 3117.264
GSM24666mtDNA "Common"-deletion subject 485.756