ProfileGDS1065 / 204907_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 63% 58% 63% 54% 53% 49% 51% 62% 57% 45% 59% 65% 62% 60% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 175.963
GSM24653Normal subject 259.658
GSM24654Normal subject 391.663
GSM24655A3243G-MELAS subject 137.854
GSM24656A3243G-MELAS subject 253.553
GSM24657A3243G-MELAS subject 360.749
GSM24658A3243G-MELAS subject 441.251
GSM24659A3243G-PEO subject 158.562
GSM24660A3243G-PEO subject 253.857
GSM24661A3243G-PEO subject 325.245
GSM24662A3243G-PEO subject 45459
GSM24663mtDNA "Common"-deletion subject 185.165
GSM24664mtDNA "Common"-deletion subject 2127.462
GSM24665mtDNA "Common"-deletion subject 3100.360
GSM24666mtDNA "Common"-deletion subject 489.457