ProfileGDS1065 / 221774_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 55% 62% 69% 69% 70% 49% 58% 62% 55% 54% 46% 63% 76% 68% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 155.855
GSM24653Normal subject 268.562
GSM24654Normal subject 3123.869
GSM24655A3243G-MELAS subject 16769
GSM24656A3243G-MELAS subject 2105.270
GSM24657A3243G-MELAS subject 361.549
GSM24658A3243G-MELAS subject 454.958
GSM24659A3243G-PEO subject 158.862
GSM24660A3243G-PEO subject 251.155
GSM24661A3243G-PEO subject 336.454
GSM24662A3243G-PEO subject 432.646
GSM24663mtDNA "Common"-deletion subject 180.563
GSM24664mtDNA "Common"-deletion subject 2250.976
GSM24665mtDNA "Common"-deletion subject 3139.668
GSM24666mtDNA "Common"-deletion subject 4158.468