ProfileGDS1065 / 208753_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 70% 74% 76% 65% 78% 79% 77% 68% 73% 72% 71% 75% 74% 81% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1105.370
GSM24653Normal subject 2117.374
GSM24654Normal subject 3184.276
GSM24655A3243G-MELAS subject 157.165
GSM24656A3243G-MELAS subject 2160.778
GSM24657A3243G-MELAS subject 3263.779
GSM24658A3243G-MELAS subject 4139.377
GSM24659A3243G-PEO subject 17568
GSM24660A3243G-PEO subject 2105.873
GSM24661A3243G-PEO subject 380.772
GSM24662A3243G-PEO subject 488.571
GSM24663mtDNA "Common"-deletion subject 1143.175
GSM24664mtDNA "Common"-deletion subject 222974
GSM24665mtDNA "Common"-deletion subject 3310.381
GSM24666mtDNA "Common"-deletion subject 4301.579