ProfileGDS1065 / 217120_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 59% 56% 63% 61% 63% 60% 59% 64% 56% 63% 65% 66% 59% 56% 50% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 164.659
GSM24653Normal subject 253.256
GSM24654Normal subject 392.963
GSM24655A3243G-MELAS subject 147.761
GSM24656A3243G-MELAS subject 277.463
GSM24657A3243G-MELAS subject 399.160
GSM24658A3243G-MELAS subject 457.259
GSM24659A3243G-PEO subject 162.964
GSM24660A3243G-PEO subject 251.656
GSM24661A3243G-PEO subject 354.163
GSM24662A3243G-PEO subject 468.265
GSM24663mtDNA "Common"-deletion subject 189.266
GSM24664mtDNA "Common"-deletion subject 2112.459
GSM24665mtDNA "Common"-deletion subject 384.556
GSM24666mtDNA "Common"-deletion subject 466.450