ProfileGDS1065 / 217768_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 97% 97% 97% 97% 97% 97% 97% 97% 97% 97% 97% 98% 98% 97% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11994.897
GSM24653Normal subject 21927.297
GSM24654Normal subject 3258397
GSM24655A3243G-MELAS subject 1964.197
GSM24656A3243G-MELAS subject 21360.797
GSM24657A3243G-MELAS subject 33036.997
GSM24658A3243G-MELAS subject 41765.397
GSM24659A3243G-PEO subject 11008.897
GSM24660A3243G-PEO subject 21422.197
GSM24661A3243G-PEO subject 31097.197
GSM24662A3243G-PEO subject 4128897
GSM24663mtDNA "Common"-deletion subject 12282.298
GSM24664mtDNA "Common"-deletion subject 23339.898
GSM24665mtDNA "Common"-deletion subject 33191.897
GSM24666mtDNA "Common"-deletion subject 43519.398