ProfileGDS1065 / 210205_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 68% 67% 49% 65% 56% 66% 65% 70% 64% 77% 69% 62% 53% 48% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 196.868
GSM24653Normal subject 285.567
GSM24654Normal subject 350.549
GSM24655A3243G-MELAS subject 157.265
GSM24656A3243G-MELAS subject 259.656
GSM24657A3243G-MELAS subject 3135.466
GSM24658A3243G-MELAS subject 47765
GSM24659A3243G-PEO subject 181.270
GSM24660A3243G-PEO subject 272.164
GSM24661A3243G-PEO subject 3101.477
GSM24662A3243G-PEO subject 483.469
GSM24663mtDNA "Common"-deletion subject 175.262
GSM24664mtDNA "Common"-deletion subject 289.953
GSM24665mtDNA "Common"-deletion subject 359.148
GSM24666mtDNA "Common"-deletion subject 4112.162