ProfileGDS1065 / 202274_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% 76% 62% 73% 60% 57% 54% 61% 60% 64% 66% 59% 62% 65% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 151.854
GSM24653Normal subject 2130.876
GSM24654Normal subject 389.162
GSM24655A3243G-MELAS subject 180.873
GSM24656A3243G-MELAS subject 269.560
GSM24657A3243G-MELAS subject 388.957
GSM24658A3243G-MELAS subject 447.754
GSM24659A3243G-PEO subject 155.661
GSM24660A3243G-PEO subject 261.460
GSM24661A3243G-PEO subject 355.564
GSM24662A3243G-PEO subject 471.166
GSM24663mtDNA "Common"-deletion subject 165.559
GSM24664mtDNA "Common"-deletion subject 213062
GSM24665mtDNA "Common"-deletion subject 3122.165
GSM24666mtDNA "Common"-deletion subject 493.858