ProfileGDS1065 / 208261_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 24% 27% 41% 40% 38% 24% 31% 43% 48% 34% 47% 19% 35% 51% 24% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111.824
GSM24653Normal subject 213.927
GSM24654Normal subject 334.841
GSM24655A3243G-MELAS subject 122.340
GSM24656A3243G-MELAS subject 228.838
GSM24657A3243G-MELAS subject 316.624
GSM24658A3243G-MELAS subject 415.331
GSM24659A3243G-PEO subject 129.243
GSM24660A3243G-PEO subject 238.248
GSM24661A3243G-PEO subject 314.634
GSM24662A3243G-PEO subject 433.147
GSM24663mtDNA "Common"-deletion subject 18.519
GSM24664mtDNA "Common"-deletion subject 241.335
GSM24665mtDNA "Common"-deletion subject 366.651
GSM24666mtDNA "Common"-deletion subject 41724