ProfileGDS1065 / 205518_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 52% 44% 43% 57% 57% 43% 38% 43% 52% 43% 54% 38% 53% 46% 54% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14952
GSM24653Normal subject 233.544
GSM24654Normal subject 338.343
GSM24655A3243G-MELAS subject 141.457
GSM24656A3243G-MELAS subject 26357
GSM24657A3243G-MELAS subject 347.643
GSM24658A3243G-MELAS subject 422.838
GSM24659A3243G-PEO subject 128.843
GSM24660A3243G-PEO subject 244.852
GSM24661A3243G-PEO subject 323.443
GSM24662A3243G-PEO subject 443.754
GSM24663mtDNA "Common"-deletion subject 126.538
GSM24664mtDNA "Common"-deletion subject 289.853
GSM24665mtDNA "Common"-deletion subject 353.946
GSM24666mtDNA "Common"-deletion subject 477.154