ProfileGDS1065 / 209288_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 77% 79% 79% 76% 81% 78% 73% 74% 83% 78% 77% 78% 83% 80% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1155.677
GSM24653Normal subject 2157.479
GSM24654Normal subject 3217.379
GSM24655A3243G-MELAS subject 189.576
GSM24656A3243G-MELAS subject 2189.281
GSM24657A3243G-MELAS subject 3258.478
GSM24658A3243G-MELAS subject 4111.773
GSM24659A3243G-PEO subject 195.174
GSM24660A3243G-PEO subject 2189.383
GSM24661A3243G-PEO subject 3106.178
GSM24662A3243G-PEO subject 4125.477
GSM24663mtDNA "Common"-deletion subject 1171.478
GSM24664mtDNA "Common"-deletion subject 2382.283
GSM24665mtDNA "Common"-deletion subject 3286.580
GSM24666mtDNA "Common"-deletion subject 4648.689