ProfileGDS1065 / 210385_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 53% 56% 50% 61% 64% 62% 30% 60% 64% 51% 51% 55% 58% 51% 54% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149.753
GSM24653Normal subject 253.456
GSM24654Normal subject 351.950
GSM24655A3243G-MELAS subject 148.961
GSM24656A3243G-MELAS subject 281.964
GSM24657A3243G-MELAS subject 3112.162
GSM24658A3243G-MELAS subject 415.130
GSM24659A3243G-PEO subject 155.260
GSM24660A3243G-PEO subject 272.864
GSM24661A3243G-PEO subject 332.451
GSM24662A3243G-PEO subject 438.551
GSM24663mtDNA "Common"-deletion subject 156.155
GSM24664mtDNA "Common"-deletion subject 2108.758
GSM24665mtDNA "Common"-deletion subject 368.851
GSM24666mtDNA "Common"-deletion subject 478.554