ProfileGDS1065 / 213235_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% 29% 57% 53% 53% 47% 34% 60% 62% 57% 55% 62% 44% 48% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 153.855
GSM24653Normal subject 215.629
GSM24654Normal subject 371.957
GSM24655A3243G-MELAS subject 136.153
GSM24656A3243G-MELAS subject 253.553
GSM24657A3243G-MELAS subject 356.747
GSM24658A3243G-MELAS subject 418.634
GSM24659A3243G-PEO subject 154.760
GSM24660A3243G-PEO subject 267.162
GSM24661A3243G-PEO subject 341.157
GSM24662A3243G-PEO subject 445.355
GSM24663mtDNA "Common"-deletion subject 176.962
GSM24664mtDNA "Common"-deletion subject 261.744
GSM24665mtDNA "Common"-deletion subject 359.648
GSM24666mtDNA "Common"-deletion subject 472.352