ProfileGDS1065 / 201462_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 56% 61% 47% 74% 55% 51% 63% 64% 40% 53% 56% 24% 50% 52% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 156.756
GSM24653Normal subject 266.361
GSM24654Normal subject 345.947
GSM24655A3243G-MELAS subject 184.374
GSM24656A3243G-MELAS subject 256.355
GSM24657A3243G-MELAS subject 368.351
GSM24658A3243G-MELAS subject 468.263
GSM24659A3243G-PEO subject 164.264
GSM24660A3243G-PEO subject 227.740
GSM24661A3243G-PEO subject 334.953
GSM24662A3243G-PEO subject 447.956
GSM24663mtDNA "Common"-deletion subject 111.324
GSM24664mtDNA "Common"-deletion subject 279.950
GSM24665mtDNA "Common"-deletion subject 369.552
GSM24666mtDNA "Common"-deletion subject 497.659