ProfileGDS1065 / 212658_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 58% 59% 67% 68% 52% 53% 65% 67% 66% 57% 62% 56% 63% 52% 61% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 162.358
GSM24653Normal subject 260.359
GSM24654Normal subject 3110.467
GSM24655A3243G-MELAS subject 162.768
GSM24656A3243G-MELAS subject 251.152
GSM24657A3243G-MELAS subject 372.353
GSM24658A3243G-MELAS subject 477.565
GSM24659A3243G-PEO subject 170.967
GSM24660A3243G-PEO subject 278.166
GSM24661A3243G-PEO subject 341.157
GSM24662A3243G-PEO subject 460.162
GSM24663mtDNA "Common"-deletion subject 158.256
GSM24664mtDNA "Common"-deletion subject 2133.363
GSM24665mtDNA "Common"-deletion subject 371.852
GSM24666mtDNA "Common"-deletion subject 4108.761