ProfileGDS1065 / 221957_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 57% 63% 57% 63% 67% 54% 66% 68% 56% 64% 59% 61% 58% 62% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 158.457
GSM24653Normal subject 272.563
GSM24654Normal subject 373.157
GSM24655A3243G-MELAS subject 152.663
GSM24656A3243G-MELAS subject 291.667
GSM24657A3243G-MELAS subject 378.454
GSM24658A3243G-MELAS subject 480.166
GSM24659A3243G-PEO subject 172.368
GSM24660A3243G-PEO subject 252.456
GSM24661A3243G-PEO subject 354.764
GSM24662A3243G-PEO subject 453.759
GSM24663mtDNA "Common"-deletion subject 171.161
GSM24664mtDNA "Common"-deletion subject 210858
GSM24665mtDNA "Common"-deletion subject 3106.862
GSM24666mtDNA "Common"-deletion subject 497.659