ProfileGDS1065 / 220150_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 30% 41% 57% 31% 56% 8% 24% 35% 42% 47% 31% 64% 23% 39% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 117.230
GSM24653Normal subject 22941
GSM24654Normal subject 370.457
GSM24655A3243G-MELAS subject 114.431
GSM24656A3243G-MELAS subject 259.756
GSM24657A3243G-MELAS subject 34.78
GSM24658A3243G-MELAS subject 410.224
GSM24659A3243G-PEO subject 119.835
GSM24660A3243G-PEO subject 229.742
GSM24661A3243G-PEO subject 327.847
GSM24662A3243G-PEO subject 41631
GSM24663mtDNA "Common"-deletion subject 181.564
GSM24664mtDNA "Common"-deletion subject 220.423
GSM24665mtDNA "Common"-deletion subject 34039
GSM24666mtDNA "Common"-deletion subject 472.352