ProfileGDS1065 / 201329_s_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 40% 39% 67% 47% 44% 52% 61% 45% 42% 52% 50% 51% 50% 52% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 129.140
GSM24653Normal subject 227.239
GSM24654Normal subject 3112.767
GSM24655A3243G-MELAS subject 128.747
GSM24656A3243G-MELAS subject 237.844
GSM24657A3243G-MELAS subject 370.352
GSM24658A3243G-MELAS subject 462.161
GSM24659A3243G-PEO subject 131.345
GSM24660A3243G-PEO subject 229.542
GSM24661A3243G-PEO subject 334.452
GSM24662A3243G-PEO subject 437.850
GSM24663mtDNA "Common"-deletion subject 14851
GSM24664mtDNA "Common"-deletion subject 277.650
GSM24665mtDNA "Common"-deletion subject 371.752
GSM24666mtDNA "Common"-deletion subject 4127.964