ProfileGDS1065 / 219050_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 64% 51% 49% 66% 61% 53% 64% 71% 60% 66% 62% 52% 61% 41% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 181.464
GSM24653Normal subject 244.751
GSM24654Normal subject 350.449
GSM24655A3243G-MELAS subject 159.166
GSM24656A3243G-MELAS subject 272.861
GSM24657A3243G-MELAS subject 373.753
GSM24658A3243G-MELAS subject 47164
GSM24659A3243G-PEO subject 184.271
GSM24660A3243G-PEO subject 260.660
GSM24661A3243G-PEO subject 359.166
GSM24662A3243G-PEO subject 462.262
GSM24663mtDNA "Common"-deletion subject 150.452
GSM24664mtDNA "Common"-deletion subject 2126.261
GSM24665mtDNA "Common"-deletion subject 343.841
GSM24666mtDNA "Common"-deletion subject 468.951