ProfileGDS1065 / 204095_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 43% 48% 47% 43% 38% 52% 44% 36% 42% 46% 44% 48% 44% 47% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 133.543
GSM24653Normal subject 238.848
GSM24654Normal subject 345.747
GSM24655A3243G-MELAS subject 125.243
GSM24656A3243G-MELAS subject 228.838
GSM24657A3243G-MELAS subject 370.352
GSM24658A3243G-MELAS subject 43144
GSM24659A3243G-PEO subject 121.536
GSM24660A3243G-PEO subject 229.442
GSM24661A3243G-PEO subject 32646
GSM24662A3243G-PEO subject 429.944
GSM24663mtDNA "Common"-deletion subject 142.248
GSM24664mtDNA "Common"-deletion subject 260.944
GSM24665mtDNA "Common"-deletion subject 356.647
GSM24666mtDNA "Common"-deletion subject 438.138