ProfileGDS1065 / 220349_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 76% 70% 58% 46% 64% 67% 65% 55% 54% 62% 71% 73% 66% 63% 61% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1143.176
GSM24653Normal subject 297.270
GSM24654Normal subject 37558
GSM24655A3243G-MELAS subject 127.546
GSM24656A3243G-MELAS subject 281.664
GSM24657A3243G-MELAS subject 3140.467
GSM24658A3243G-MELAS subject 476.765
GSM24659A3243G-PEO subject 145.455
GSM24660A3243G-PEO subject 248.754
GSM24661A3243G-PEO subject 351.462
GSM24662A3243G-PEO subject 489.171
GSM24663mtDNA "Common"-deletion subject 112673
GSM24664mtDNA "Common"-deletion subject 2151.566
GSM24665mtDNA "Common"-deletion subject 3112.163
GSM24666mtDNA "Common"-deletion subject 4106.661