ProfileGDS1065 / 221647_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 79% 83% 78% 83% 80% 85% 80% 79% 75% 75% 77% 76% 81% 82% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1173.779
GSM24653Normal subject 2211.983
GSM24654Normal subject 3199.878
GSM24655A3243G-MELAS subject 1131.183
GSM24656A3243G-MELAS subject 2174.980
GSM24657A3243G-MELAS subject 3399.885
GSM24658A3243G-MELAS subject 4170.980
GSM24659A3243G-PEO subject 1123.579
GSM24660A3243G-PEO subject 2117.675
GSM24661A3243G-PEO subject 389.975
GSM24662A3243G-PEO subject 4126.277
GSM24663mtDNA "Common"-deletion subject 1152.476
GSM24664mtDNA "Common"-deletion subject 2333.581
GSM24665mtDNA "Common"-deletion subject 332382
GSM24666mtDNA "Common"-deletion subject 4272.678