ProfileGDS1065 / 205760_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 54% 56% 42% 54% 50% 54% 53% 61% 58% 47% 55% 45% 52% 51% 54% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 152.554
GSM24653Normal subject 254.556
GSM24654Normal subject 336.942
GSM24655A3243G-MELAS subject 137.754
GSM24656A3243G-MELAS subject 248.150
GSM24657A3243G-MELAS subject 375.754
GSM24658A3243G-MELAS subject 444.253
GSM24659A3243G-PEO subject 155.861
GSM24660A3243G-PEO subject 257.458
GSM24661A3243G-PEO subject 327.247
GSM24662A3243G-PEO subject 446.155
GSM24663mtDNA "Common"-deletion subject 136.445
GSM24664mtDNA "Common"-deletion subject 286.852
GSM24665mtDNA "Common"-deletion subject 367.451
GSM24666mtDNA "Common"-deletion subject 477.454