ProfileGDS1065 / 207680_x_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 54% 52% 20% 51% 43% 41% 49% 53% 45% 49% 44% 39% 38% 46% 34% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 153.154
GSM24653Normal subject 246.252
GSM24654Normal subject 39.820
GSM24655A3243G-MELAS subject 133.251
GSM24656A3243G-MELAS subject 235.343
GSM24657A3243G-MELAS subject 343.241
GSM24658A3243G-MELAS subject 438.149
GSM24659A3243G-PEO subject 141.953
GSM24660A3243G-PEO subject 233.745
GSM24661A3243G-PEO subject 330.349
GSM24662A3243G-PEO subject 429.544
GSM24663mtDNA "Common"-deletion subject 128.139
GSM24664mtDNA "Common"-deletion subject 248.538
GSM24665mtDNA "Common"-deletion subject 355.246
GSM24666mtDNA "Common"-deletion subject 43134