ProfileGDS1065 / 211749_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 67% 62% 90% 79% 80% 68% 77% 70% 77% 63% 67% 71% 83% 84% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 189.167
GSM24653Normal subject 267.562
GSM24654Normal subject 3506.890
GSM24655A3243G-MELAS subject 1107.379
GSM24656A3243G-MELAS subject 2181.480
GSM24657A3243G-MELAS subject 3146.868
GSM24658A3243G-MELAS subject 413977
GSM24659A3243G-PEO subject 180.570
GSM24660A3243G-PEO subject 2128.677
GSM24661A3243G-PEO subject 354.163
GSM24662A3243G-PEO subject 474.767
GSM24663mtDNA "Common"-deletion subject 1112.871
GSM24664mtDNA "Common"-deletion subject 2380.483
GSM24665mtDNA "Common"-deletion subject 3391.184
GSM24666mtDNA "Common"-deletion subject 4274.178