ProfileGDS1065 / 219161_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 54% 51% 54% 45% 54% 58% 58% 46% 49% 51% 49% 51% 57% 57% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 153.354
GSM24653Normal subject 245.251
GSM24654Normal subject 364.154
GSM24655A3243G-MELAS subject 127.145
GSM24656A3243G-MELAS subject 254.254
GSM24657A3243G-MELAS subject 391.158
GSM24658A3243G-MELAS subject 455.758
GSM24659A3243G-PEO subject 132.946
GSM24660A3243G-PEO subject 239.649
GSM24661A3243G-PEO subject 332.951
GSM24662A3243G-PEO subject 435.649
GSM24663mtDNA "Common"-deletion subject 148.351
GSM24664mtDNA "Common"-deletion subject 2102.957
GSM24665mtDNA "Common"-deletion subject 38657
GSM24666mtDNA "Common"-deletion subject 4119.563