ProfileGDS1065 / 221402_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 75% 72% 62% 78% 72% 60% 67% 76% 71% 72% 72% 72% 71% 66% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1138.875
GSM24653Normal subject 2106.872
GSM24654Normal subject 391.462
GSM24655A3243G-MELAS subject 1100.878
GSM24656A3243G-MELAS subject 2115.272
GSM24657A3243G-MELAS subject 3102.560
GSM24658A3243G-MELAS subject 485.567
GSM24659A3243G-PEO subject 1103.376
GSM24660A3243G-PEO subject 298.171
GSM24661A3243G-PEO subject 380.272
GSM24662A3243G-PEO subject 496.172
GSM24663mtDNA "Common"-deletion subject 1121.272
GSM24664mtDNA "Common"-deletion subject 2190.971
GSM24665mtDNA "Common"-deletion subject 3127.366
GSM24666mtDNA "Common"-deletion subject 4123.464