ProfileGDS1065 / 217044_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 72% 39% 58% 36% 35% 69% 70% 66% 53% 40% 75% 66% 47% 70% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1118.172
GSM24653Normal subject 226.639
GSM24654Normal subject 374.858
GSM24655A3243G-MELAS subject 118.336
GSM24656A3243G-MELAS subject 225.435
GSM24657A3243G-MELAS subject 3155.869
GSM24658A3243G-MELAS subject 495.370
GSM24659A3243G-PEO subject 168.266
GSM24660A3243G-PEO subject 246.253
GSM24661A3243G-PEO subject 320.640
GSM24662A3243G-PEO subject 411075
GSM24663mtDNA "Common"-deletion subject 189.566
GSM24664mtDNA "Common"-deletion subject 269.947
GSM24665mtDNA "Common"-deletion subject 3154.970
GSM24666mtDNA "Common"-deletion subject 476.653