ProfileGDS1065 / 212772_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 76% 75% 70% 74% 73% 67% 61% 72% 76% 73% 76% 77% 73% 71% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1149.376
GSM24653Normal subject 2124.275
GSM24654Normal subject 3132.470
GSM24655A3243G-MELAS subject 181.474
GSM24656A3243G-MELAS subject 2120.973
GSM24657A3243G-MELAS subject 314167
GSM24658A3243G-MELAS subject 46361
GSM24659A3243G-PEO subject 187.372
GSM24660A3243G-PEO subject 2126.676
GSM24661A3243G-PEO subject 383.573
GSM24662A3243G-PEO subject 4119.676
GSM24663mtDNA "Common"-deletion subject 1159.577
GSM24664mtDNA "Common"-deletion subject 221273
GSM24665mtDNA "Common"-deletion subject 3167.871
GSM24666mtDNA "Common"-deletion subject 4184.771