ProfileGDS1065 / 206252_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 19% 42% 11% 8% 25% 21% 30% 42% 35% 26% 20% 7% 6% 9% 24% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.519
GSM24653Normal subject 230.442
GSM24654Normal subject 34.911
GSM24655A3243G-MELAS subject 138
GSM24656A3243G-MELAS subject 214.125
GSM24657A3243G-MELAS subject 313.321
GSM24658A3243G-MELAS subject 414.730
GSM24659A3243G-PEO subject 127.942
GSM24660A3243G-PEO subject 221.935
GSM24661A3243G-PEO subject 39.226
GSM24662A3243G-PEO subject 47.820
GSM24663mtDNA "Common"-deletion subject 13.27
GSM24664mtDNA "Common"-deletion subject 25.36
GSM24665mtDNA "Common"-deletion subject 35.69
GSM24666mtDNA "Common"-deletion subject 417.224