ProfileGDS1065 / 221008_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 55% 16% 51% 54% 50% 41% 47% 51% 46% 53% 46% 61% 46% 63% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 155.355
GSM24653Normal subject 26.416
GSM24654Normal subject 354.151
GSM24655A3243G-MELAS subject 137.954
GSM24656A3243G-MELAS subject 246.650
GSM24657A3243G-MELAS subject 342.541
GSM24658A3243G-MELAS subject 435.347
GSM24659A3243G-PEO subject 139.551
GSM24660A3243G-PEO subject 235.946
GSM24661A3243G-PEO subject 335.753
GSM24662A3243G-PEO subject 43246
GSM24663mtDNA "Common"-deletion subject 171.561
GSM24664mtDNA "Common"-deletion subject 267.446
GSM24665mtDNA "Common"-deletion subject 3109.863
GSM24666mtDNA "Common"-deletion subject 434.135