ProfileGDS1065 / 204264_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 63% 71% 63% 79% 72% 80% 72% 64% 72% 73% 78% 73% 75% 64% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 176.363
GSM24653Normal subject 2105.371
GSM24654Normal subject 393.563
GSM24655A3243G-MELAS subject 1104.679
GSM24656A3243G-MELAS subject 2116.372
GSM24657A3243G-MELAS subject 3287.480
GSM24658A3243G-MELAS subject 410572
GSM24659A3243G-PEO subject 162.764
GSM24660A3243G-PEO subject 299.572
GSM24661A3243G-PEO subject 383.873
GSM24662A3243G-PEO subject 413078
GSM24663mtDNA "Common"-deletion subject 1124.773
GSM24664mtDNA "Common"-deletion subject 2234.475
GSM24665mtDNA "Common"-deletion subject 311964
GSM24666mtDNA "Common"-deletion subject 4179.571