ProfileGDS1065 / 202484_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 78% 71% 81% 79% 77% 78% 79% 72% 77% 72% 63% 79% 81% 82% 80% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1163.278
GSM24653Normal subject 210571
GSM24654Normal subject 3239.881
GSM24655A3243G-MELAS subject 1106.779
GSM24656A3243G-MELAS subject 2146.877
GSM24657A3243G-MELAS subject 3248.278
GSM24658A3243G-MELAS subject 4162.179
GSM24659A3243G-PEO subject 185.872
GSM24660A3243G-PEO subject 2133.377
GSM24661A3243G-PEO subject 380.772
GSM24662A3243G-PEO subject 463.463
GSM24663mtDNA "Common"-deletion subject 1181.179
GSM24664mtDNA "Common"-deletion subject 2339.881
GSM24665mtDNA "Common"-deletion subject 3317.882
GSM24666mtDNA "Common"-deletion subject 4322.480