ProfileGDS1065 / 57703_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 43% 35% 43% 37% 41% 38% 34% 42% 37% 41% 41% 40% 34% 40% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132.943
GSM24653Normal subject 222.335
GSM24654Normal subject 339.443
GSM24655A3243G-MELAS subject 119.437
GSM24656A3243G-MELAS subject 233.441
GSM24657A3243G-MELAS subject 336.838
GSM24658A3243G-MELAS subject 418.734
GSM24659A3243G-PEO subject 127.442
GSM24660A3243G-PEO subject 223.837
GSM24661A3243G-PEO subject 321.141
GSM24662A3243G-PEO subject 426.441
GSM24663mtDNA "Common"-deletion subject 129.740
GSM24664mtDNA "Common"-deletion subject 239.634
GSM24665mtDNA "Common"-deletion subject 343.140
GSM24666mtDNA "Common"-deletion subject 43838