ProfileGDS1065 / 210048_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 56% 45% 53% 59% 46% 49% 52% 47% 44% 52% 48% 49% 53% 48% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 156.856
GSM24653Normal subject 235.345
GSM24654Normal subject 359.153
GSM24655A3243G-MELAS subject 145.559
GSM24656A3243G-MELAS subject 240.146
GSM24657A3243G-MELAS subject 36149
GSM24658A3243G-MELAS subject 443.352
GSM24659A3243G-PEO subject 133.747
GSM24660A3243G-PEO subject 233.144
GSM24661A3243G-PEO subject 333.752
GSM24662A3243G-PEO subject 434.648
GSM24663mtDNA "Common"-deletion subject 143.149
GSM24664mtDNA "Common"-deletion subject 289.453
GSM24665mtDNA "Common"-deletion subject 360.748
GSM24666mtDNA "Common"-deletion subject 460.648