ProfileGDS1065 / 201467_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 9% 16% 19% 16% 8% 12% 18% 26% 10% 12% 13% 19% 36% 10% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149
GSM24653Normal subject 26.416
GSM24654Normal subject 39.319
GSM24655A3243G-MELAS subject 15.716
GSM24656A3243G-MELAS subject 24.38
GSM24657A3243G-MELAS subject 36.612
GSM24658A3243G-MELAS subject 46.418
GSM24659A3243G-PEO subject 112.226
GSM24660A3243G-PEO subject 24.410
GSM24661A3243G-PEO subject 33.712
GSM24662A3243G-PEO subject 44.513
GSM24663mtDNA "Common"-deletion subject 18.519
GSM24664mtDNA "Common"-deletion subject 243.236
GSM24665mtDNA "Common"-deletion subject 35.910
GSM24666mtDNA "Common"-deletion subject 418.525