ProfileGDS1065 / 219038_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 75% 68% 68% 67% 68% 67% 69% 73% 71% 75% 67% 69% 72% 69% 75% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1138.275
GSM24653Normal subject 288.368
GSM24654Normal subject 3120.468
GSM24655A3243G-MELAS subject 160.467
GSM24656A3243G-MELAS subject 295.268
GSM24657A3243G-MELAS subject 3137.367
GSM24658A3243G-MELAS subject 493.469
GSM24659A3243G-PEO subject 191.973
GSM24660A3243G-PEO subject 298.871
GSM24661A3243G-PEO subject 39075
GSM24662A3243G-PEO subject 473.767
GSM24663mtDNA "Common"-deletion subject 1103.169
GSM24664mtDNA "Common"-deletion subject 2208.372
GSM24665mtDNA "Common"-deletion subject 3149.969
GSM24666mtDNA "Common"-deletion subject 4228.575