ProfileGDS1065 / 205697_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 39% 27% 37% 35% 43% 37% 53% 39% 34% 20% 48% 24% 14% 54% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 128.539
GSM24653Normal subject 213.527
GSM24654Normal subject 329.437
GSM24655A3243G-MELAS subject 117.435
GSM24656A3243G-MELAS subject 236.343
GSM24657A3243G-MELAS subject 335.737
GSM24658A3243G-MELAS subject 444.153
GSM24659A3243G-PEO subject 124.639
GSM24660A3243G-PEO subject 220.734
GSM24661A3243G-PEO subject 36.520
GSM24662A3243G-PEO subject 435.148
GSM24663mtDNA "Common"-deletion subject 111.224
GSM24664mtDNA "Common"-deletion subject 210.114
GSM24665mtDNA "Common"-deletion subject 376.454
GSM24666mtDNA "Common"-deletion subject 413.921