ProfileGDS1065 / 201070_x_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 66% 63% 73% 61% 68% 63% 65% 70% 64% 71% 63% 66% 70% 65% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 186.366
GSM24653Normal subject 271.463
GSM24654Normal subject 3154.673
GSM24655A3243G-MELAS subject 147.861
GSM24656A3243G-MELAS subject 293.468
GSM24657A3243G-MELAS subject 3117.863
GSM24658A3243G-MELAS subject 476.365
GSM24659A3243G-PEO subject 17970
GSM24660A3243G-PEO subject 271.664
GSM24661A3243G-PEO subject 375.871
GSM24662A3243G-PEO subject 46363
GSM24663mtDNA "Common"-deletion subject 188.566
GSM24664mtDNA "Common"-deletion subject 2180.870
GSM24665mtDNA "Common"-deletion subject 3122.765
GSM24666mtDNA "Common"-deletion subject 494.658