ProfileGDS1065 / 205539_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 52% 51% 58% 53% 54% 48% 59% 53% 53% 57% 49% 56% 61% 64% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 147.252
GSM24653Normal subject 24551
GSM24654Normal subject 373.458
GSM24655A3243G-MELAS subject 136.153
GSM24656A3243G-MELAS subject 255.354
GSM24657A3243G-MELAS subject 359.148
GSM24658A3243G-MELAS subject 456.559
GSM24659A3243G-PEO subject 141.553
GSM24660A3243G-PEO subject 247.153
GSM24661A3243G-PEO subject 341.357
GSM24662A3243G-PEO subject 436.349
GSM24663mtDNA "Common"-deletion subject 157.456
GSM24664mtDNA "Common"-deletion subject 2125.361
GSM24665mtDNA "Common"-deletion subject 3116.764
GSM24666mtDNA "Common"-deletion subject 488.256