ProfileGDS1065 / 207800_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 40% 40% 36% 43% 38% 31% 32% 24% 45% 32% 35% 17% 52% 31% 24% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 128.840
GSM24653Normal subject 227.740
GSM24654Normal subject 32836
GSM24655A3243G-MELAS subject 124.443
GSM24656A3243G-MELAS subject 228.938
GSM24657A3243G-MELAS subject 326.231
GSM24658A3243G-MELAS subject 417.232
GSM24659A3243G-PEO subject 111.424
GSM24660A3243G-PEO subject 233.745
GSM24661A3243G-PEO subject 313.132
GSM24662A3243G-PEO subject 420.135
GSM24663mtDNA "Common"-deletion subject 17.117
GSM24664mtDNA "Common"-deletion subject 286.552
GSM24665mtDNA "Common"-deletion subject 327.631
GSM24666mtDNA "Common"-deletion subject 416.624