ProfileGDS1065 / 217493_x_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 72% 59% 65% 70% 69% 69% 63% 62% 70% 73% 80% 73% 67% 62% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1115.872
GSM24653Normal subject 260.459
GSM24654Normal subject 3102.465
GSM24655A3243G-MELAS subject 170.570
GSM24656A3243G-MELAS subject 29969
GSM24657A3243G-MELAS subject 3153.969
GSM24658A3243G-MELAS subject 469.463
GSM24659A3243G-PEO subject 157.762
GSM24660A3243G-PEO subject 292.370
GSM24661A3243G-PEO subject 381.973
GSM24662A3243G-PEO subject 4143.780
GSM24663mtDNA "Common"-deletion subject 1123.973
GSM24664mtDNA "Common"-deletion subject 2160.367
GSM24665mtDNA "Common"-deletion subject 3105.762
GSM24666mtDNA "Common"-deletion subject 416769