ProfileGDS1065 / 218948_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 67% 62% 69% 74% 73% 59% 65% 61% 42% 52% 65% 73% 68% 70% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 193.367
GSM24653Normal subject 269.662
GSM24654Normal subject 3126.869
GSM24655A3243G-MELAS subject 181.774
GSM24656A3243G-MELAS subject 2117.973
GSM24657A3243G-MELAS subject 393.559
GSM24658A3243G-MELAS subject 476.865
GSM24659A3243G-PEO subject 15661
GSM24660A3243G-PEO subject 230.342
GSM24661A3243G-PEO subject 333.652
GSM24662A3243G-PEO subject 468.365
GSM24663mtDNA "Common"-deletion subject 1126.673
GSM24664mtDNA "Common"-deletion subject 2168.668
GSM24665mtDNA "Common"-deletion subject 3153.570
GSM24666mtDNA "Common"-deletion subject 4145.467